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..
Clearance details
- Applicant
- Welch Allyn, Inc.
- Product code
- Code HOO
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Skaneateles Falls, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.