SPAN-AID BRIDGING PILLOW SYSTEM— 510(k) K801518

Name: FDA 510(k) clearance K801518
Creator: U.S. Food and Drug Administration
Published: 1980-08-04

Substantially Equivalent

Span-America Medical Systems, Inc.

FDA 510(k) clearance K801518 for SPAN-AID BRIDGING PILLOW SYSTEM, Substantially Equivalent on 1980-08-04. Applicant: Span-America Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Span-America Medical Systems, Inc.
Product code: Code HKX
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 1980-07-01
Decision date: 1980-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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