The following data is part of a premarket notification filed by Olympus America, Inc. with the FDA for Olypus Fg Series Grasping Forceps.
| Device ID | K962533 |
| 510k Number | K962533 |
| Device Name: | OLYPUS FG SERIES GRASPING FORCEPS |
| Classification | Bronchoscope (flexible Or Rigid) |
| Applicant | OLYMPUS AMERICA, INC. TWO CORPORATE CENTER DR. Melville, NY 11747 -3157 |
| Contact | Barry E Sands |
| Correspondent | Barry E Sands OLYMPUS AMERICA, INC. TWO CORPORATE CENTER DR. Melville, NY 11747 -3157 |
| Product Code | EOQ |
| CFR Regulation Number | 874.4680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-28 |
| Decision Date | 1996-08-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 14953170048989 | K962533 | 000 |
| 14953170032131 | K962533 | 000 |
| 14953170032162 | K962533 | 000 |
| 14953170032193 | K962533 | 000 |
| 14953170032223 | K962533 | 000 |
| 14953170032254 | K962533 | 000 |
| 14953170032285 | K962533 | 000 |
| 14953170032315 | K962533 | 000 |
| 14953170032353 | K962533 | 000 |
| 14953170032100 | K962533 | 000 |