The following data is part of a premarket notification filed by Weck Endoscopy with the FDA for Endoscope And Accessories.
| Device ID | K930082 |
| 510k Number | K930082 |
| Device Name: | ENDOSCOPE AND ACCESSORIES |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | WECK ENDOSCOPY P.O. BOX 12600 WECK DR. Research Triangle Park, NC 27709 |
| Contact | Joseph A Mertis |
| Correspondent | Joseph A Mertis WECK ENDOSCOPY P.O. BOX 12600 WECK DR. Research Triangle Park, NC 27709 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-07 |
| Decision Date | 1993-03-15 |