IM COLLAGEN SHIELD— 510(k) K896449

Substantially Equivalent

Intermedical, Inc.

FDA 510(k) clearance K896449 for IM COLLAGEN SHIELD, Substantially Equivalent on 1990-05-24. Applicant: Intermedical, Inc.. Device class: 1.

Clearance details

Applicant: Intermedical, Inc.
Product code: Code MOE
Device class: Class 1
Regulation: 21 CFR 886.4750
Advisory panel: Ophthalmic
Date received: 1989-11-09
Decision date: 1990-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Safety Harbor, FL, US

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Recent devices under product code MOE

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K913148 — COLLAGEN SHIELD FOR ACUTE CARE1991-10-15
K905825 — COLLAGEN SHIELD, VARIOUS MODELS1991-06-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.