LASER CENTERING DEVICE— 510(k) K872747

Substantially Equivalent

Innomed Corp.

FDA 510(k) clearance K872747 for LASER CENTERING DEVICE, Substantially Equivalent on 1987-09-04. Applicant: Innomed Corp..

Clearance details

Applicant: Innomed Corp.
Product code: Code HMR
Advisory panel: Ophthalmic
Date received: 1987-07-13
Decision date: 1987-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

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