WELCH ALLYN GLAUCOMA DETECTOR— 510(k) K941723
Substantially EquivalentWelch Allyn, Inc.
FDA 510(k) clearance K941723 for WELCH ALLYN GLAUCOMA DETECTOR, Substantially Equivalent on 1994-06-06. Applicant: Welch Allyn, Inc.. Device class: 1.
Clearance details
- Applicant
- Welch Allyn, Inc.
- Product code
- Code HOO
- Device class
- Class 1
- Regulation
- 21 CFR 886.1605
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Skaneateles Falls, NY, US
Recent devices under product code HOO
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