FDA 510(k)

PMS ANGIO DRAPE

K-Number: K890471 · 1989-02-27

Decision Date1989-02-27

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PMS ANGIO DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Services. It received FDA 510(k) clearance on 1989-02-27 under 510(k) number K890471. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMS ANGIO DRAPE?

PMS ANGIO DRAPE is a medical device that received FDA 510(k) clearance on 1989-02-27. The listed applicant is Professional Medical Services. The 510(k) number is K890471.

When did PMS ANGIO DRAPE receive FDA 510(k) clearance?

PMS ANGIO DRAPE received FDA 510(k) clearance on 1989-02-27, under 510(k) number K890471.

Who is the listed applicant for PMS ANGIO DRAPE?

The FDA 510(k) record lists Professional Medical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PMS ANGIO DRAPE?

The FDA product code for PMS ANGIO DRAPE is KKX.

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Other records listing Professional Medical Services as applicant

K913094DISPOSABLE SLIDE VALVE MANIFOLD K910378PRESSURE MONITORING EXTENSION LINE K904508CONDOR ANALOG INFLATION SYRINGE K904954CONDOR DIGITAL INFLATION SYRINGE K902606RADIOPAQUE RULER K884577PROCEDURE READY TRAYS

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Related Devices (Code: KKX)

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Official Source

View on FDA Database →

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