FDA 510(k) · Life Sciences Manufacturing
K896500: CWD/PPG MODULE (Life Sciences Manufacturing, Inc.)
Life Sciences Manufacturing, Inc. received FDA 510(k) K896500 for CWD/PPG MODULE, with a decision date of Jul 18, 1990 (substantially equivalent).
Prescription or OTC: Unknown (no FDA document we parsed states it).
FDA facts
| FDA number | K896500 |
|---|---|
| Pathway | 510(k) |
| Applicant | Life Sciences Manufacturing, Inc. |
| Device name | CWD/PPG MODULE |
| Product code | JOM: Plethysmograph, Photoelectric, Pneumatic Or Hydraulic |
| Regulation (21 CFR) | 870.2780 |
| Device class | Class 2 |
| Date received | Nov 14, 1989 |
| Decision date | Jul 18, 1990 |
| Decision | Substantially Equivalent (SESE) |
| 510(k) type | Traditional |
Source: openFDA device 510(k) data, data through Oct 26, 2026.
Indications for use parsed from FDA documents
We could not extract the indications for this record (no summary PDF was processed). Check the FDA record for its summary or statement.
Predicates parsed from FDA documents
No predicate numbers were parsed for this record. The FDA summary, if available, names the predicate.
ChatPPG interpretation
A 510(k) decision of "substantially equivalent" means FDA found the device as safe and effective as a legally marketed predicate. FDA's word for this is cleared, not approved. The clearance covers the device and indications in this submission; it does not extend to other features or versions of the same product that were not part of it. See FDA cleared vs approved.
Product code JOM is "Plethysmograph, Photoelectric, Pneumatic Or Hydraulic", class 2, 21 CFR 870.2780.
Our labels for filtering: claim Heart rate / pulse, sensor Other. These are heuristics, not FDA fields.