SHOW'RBAG— 510(k) K822059

Name: FDA 510(k) clearance K822059
Creator: U.S. Food and Drug Administration
Published: 1982-07-22

Substantially Equivalent

The Healthcare Group Laboratories, Inc.

FDA 510(k) clearance K822059 for SHOW'RBAG, Substantially Equivalent on 1982-07-22. Applicant: The Healthcare Group Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: The Healthcare Group Laboratories, Inc.
Product code: Code LGF
Device class: Class 1
Regulation: 21 CFR 888.5940
Advisory panel: Orthopedic
Date received: 1982-07-13
Decision date: 1982-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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