CAMERA, GAMMA— 510(k) K780060

Name: FDA 510(k) clearance K780060
Creator: U.S. Food and Drug Administration
Published: 1978-01-26

Substantially Equivalent

Ackerman-Schmehl Industries, Inc.

FDA 510(k) clearance K780060 for CAMERA, GAMMA, Substantially Equivalent on 1978-01-26. Applicant: Ackerman-Schmehl Industries, Inc.. Device class: 1.

Clearance details

Applicant: Ackerman-Schmehl Industries, Inc.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 1978-01-11
Decision date: 1978-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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