FDA 510(k)

PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD

K-Number: K890878 · 1989-03-14

Decision Date1989-03-14

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Imaging, Inc.. It received FDA 510(k) clearance on 1989-03-14 under 510(k) number K890878. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD?

PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is U.S. Imaging, Inc.. The 510(k) number is K890878.

When did PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD receive FDA 510(k) clearance?

PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD received FDA 510(k) clearance on 1989-03-14, under 510(k) number K890878.

Who is the listed applicant for PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD?

The FDA 510(k) record lists U.S. Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD?

The FDA product code for PHOTOMULITPLIER TUBE INTERFACE P.C. BOARD is JAA.

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Other records listing U.S. Imaging, Inc. as applicant

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Related Devices (Code: JAA)

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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.