Wall Charger, Model #79111
510(k) K770770
Wall Charger, Model #79111 is a Class I device made by Welch Allyn, Inc., cleared under FDA 510(k) K770770 on 29 Apr 1977, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK770770 | Date29 Apr 1977 | StatusActive |
Official records
- FDA 510(k) database K770770
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ERA
- Device class
- Class I
- Regulation
- 21 CFR Part 874.4770
- Advisory committee
- Ear, Nose, Throat
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code ERA (Otoscope).
- H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG by Rudolf Riester GmbH & Co. KG
- BETA X Otoscope 3x B-130.28.330 by Heine Optotechnik GmbH & Co. KG
- Diagnostix™ 543122L by American Diagnostic Corporation
- K 180 OTOSCOPE 2,5 V B-001.11.550 by Heine Optotechnik GmbH & Co. KG
- OTOSCOPE A-34 by Neitz Instruments Co., Ltd.
- VIDEO OTOSCOPE by JEDMED Instrument Company
- DISPOSA-SPEC by PLASTI-PRODUCTS, INC.
- RI-SCOPE (S) by Rudolf Riester GmbH & Co. KG
- MedRx Video Otoscope by Medrx, Inc.
- 1-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON B by Artiberia