The following data is part of a premarket notification filed by National Advanced Endoscopy Devices, Inc. with the FDA for Aed Arthroscope.
| Device ID | K991656 |
| 510k Number | K991656 |
| Device Name: | AED ARTHROSCOPE |
| Classification | Arthroscope |
| Applicant | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. 10801 NATIONAL BLVD., #603 Los Angeles, CA 90064 |
| Contact | Gayle M Butler |
| Correspondent | Gayle M Butler NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. 10801 NATIONAL BLVD., #603 Los Angeles, CA 90064 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-05-13 |
| Decision Date | 1999-12-02 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00848657019378 | K991656 | 000 |
| 00848657087230 | K991656 | 000 |
| 00848657074711 | K991656 | 000 |
| 00848657074667 | K991656 | 000 |
| 00848657074636 | K991656 | 000 |
| 00848657074544 | K991656 | 000 |
| 00848657074537 | K991656 | 000 |
| 00848657074520 | K991656 | 000 |
| 00848657074513 | K991656 | 000 |
| 00848657072380 | K991656 | 000 |
| 00848657071451 | K991656 | 000 |
| 00848657071437 | K991656 | 000 |
| 00848657070812 | K991656 | 000 |
| 00848657023153 | K991656 | 000 |
| 00848657087261 | K991656 | 000 |
| 00848657087285 | K991656 | 000 |
| 00848657087308 | K991656 | 000 |
| 00848657019361 | K991656 | 000 |
| 00848657019354 | K991656 | 000 |
| 00848657019347 | K991656 | 000 |
| 00848657019330 | K991656 | 000 |
| 00848657019323 | K991656 | 000 |
| 00848657019316 | K991656 | 000 |
| 00848657019309 | K991656 | 000 |
| 00848657014229 | K991656 | 000 |
| 00848657014038 | K991656 | 000 |
| 00848657087414 | K991656 | 000 |
| 00848657087391 | K991656 | 000 |
| 00848657087377 | K991656 | 000 |
| 00848657087353 | K991656 | 000 |
| 00848657023146 | K991656 | 000 |