The following data is part of a premarket notification filed by Welch Allyn, Inc. with the FDA for Wall Transformers 74710 & 74910.
Device ID | K771864 |
510k Number | K771864 |
Device Name: | WALL TRANSFORMERS 74710 & 74910 |
Classification | Transformer, Endoscope |
Applicant | WELCH ALLYN, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GCW |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1977-10-03 |
Decision Date | 1977-11-22 |