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FDA 510(k)

CAMERA, GAMMA

K-Number: K780060 · 1978-01-26

ApplicantAckerman-Schmehl Industries, Inc.
Decision Date1978-01-26
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAMERA, GAMMA is the device name listed in this FDA 510(k) record. The listed applicant is Ackerman-Schmehl Industries, Inc.. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K780060. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMERA, GAMMA?

CAMERA, GAMMA is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Ackerman-Schmehl Industries, Inc.. The 510(k) number is K780060.

When did CAMERA, GAMMA receive FDA 510(k) clearance?

CAMERA, GAMMA received FDA 510(k) clearance on 1978-01-26, under 510(k) number K780060.

Who is the listed applicant for CAMERA, GAMMA?

The FDA 510(k) record lists Ackerman-Schmehl Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAMERA, GAMMA?

The FDA product code for CAMERA, GAMMA is IYX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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