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FDA 510(k)

P2020 MOBILE C-ARM IMAGE INTENSIFIER

K-Number: K874905 · 1988-02-26

ApplicantPhoto Medic Equipment, Inc.
Decision Date1988-02-26
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

P2020 MOBILE C-ARM IMAGE INTENSIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Photo Medic Equipment, Inc.. It received FDA 510(k) clearance on 1988-02-26 under 510(k) number K874905. 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 P2020 MOBILE C-ARM IMAGE INTENSIFIER?

P2020 MOBILE C-ARM IMAGE INTENSIFIER is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Photo Medic Equipment, Inc.. The 510(k) number is K874905.

When did P2020 MOBILE C-ARM IMAGE INTENSIFIER receive FDA 510(k) clearance?

P2020 MOBILE C-ARM IMAGE INTENSIFIER received FDA 510(k) clearance on 1988-02-26, under 510(k) number K874905.

Who is the listed applicant for P2020 MOBILE C-ARM IMAGE INTENSIFIER?

The FDA 510(k) record lists Photo Medic Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P2020 MOBILE C-ARM IMAGE INTENSIFIER?

The FDA product code for P2020 MOBILE C-ARM IMAGE INTENSIFIER is JAA.

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Related Devices (Code: JAA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging CorporationK251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLCK242488Soteria E-ViewOmega Medical Imaging, LLCK242948Adora DRFi (04550010)Nrt X-Ray A/SK233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech AmericaK233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

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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