AMPU-PAK— 510(k) K860511

Name: FDA 510(k) clearance K860511
Creator: U.S. Food and Drug Administration
Published: 1986-08-04

Substantially Equivalent

Ammerman Medical Enterprises, Inc.

FDA 510(k) clearance K860511 for AMPU-PAK, Substantially Equivalent on 1986-08-04. Applicant: Ammerman Medical Enterprises, Inc.. Device class: Unclassified.

Clearance details

Applicant: Ammerman Medical Enterprises, Inc.
Product code: Code LPZ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1986-02-11
Decision date: 1986-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

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