Gm Engineering, Inc.
La Verne, CA, US
Gm Engineering, Inc. appears in FDA device records in La Verne, CA. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Gm Engineering, Inc. between 1993 and 1995. The busiest year on record is 1994, with 5. The most recent is 1995, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 3 |
| 1994 | 5 |
| 1995 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K953348 | ARTICULATING RETRACTOR TISSUE RETRACTORS | GCJ | Substantially Equivalent | |
| K942626 | CONTINUOUS FLOW BIOPSY PROBE | FDC | Substantially Equivalent | |
| K932394 | BERNSTEIN(TM) UTERINE MANIPULATOR | LKF | Substantially Equivalent | |
| K941661 | GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT | EQH | Substantially Equivalent | |
| K942703 | GM REUSABLE AND DISPOSABLE TROCAR AND GM REUSABLE AND DISPOSABLE ULTRA-LIGHT CANNULA | GCJ | Substantially Equivalent | |
| K941662 | GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHT | EQH | Substantially Equivalent | |
| K941660 | GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT | KYH | Substantially Equivalent | |
| K933962 | GM CONTINUOUS FLOW BIOPSY PROBE | FDC | Substantially Equivalent | |
| K934035 | GM MONOPOLAR/FRAZIER SUCTION PROBE | GEI | Substantially Equivalent | |
| K930611 | TRUE FLOW(TM) VALVE | GEX | Substantially Equivalent | |
| K931398 | GM SWIVEL VIDEO (TM) IRRIGATOR | KAR | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain