The following data is part of a premarket notification filed by Welch Allyn, Inc. with the FDA for Video Sigmoidoscope.
| Device ID | K950429 |
| 510k Number | K950429 |
| Device Name: | VIDEO SIGMOIDOSCOPE |
| Classification | Sigmoidoscope And Accessories, Flexible/rigid |
| Applicant | WELCH ALLYN, INC. 4341 SOUTH STATE ST. RD. P.O. BOX 220 Skaneateles Falls, NY 13153 -0220 |
| Contact | Lawrence E Marocco |
| Correspondent | Lawrence E Marocco WELCH ALLYN, INC. 4341 SOUTH STATE ST. RD. P.O. BOX 220 Skaneateles Falls, NY 13153 -0220 |
| Product Code | FAM |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-02 |
| Decision Date | 1995-08-01 |