FDA 510(k)

VIRAPUMP II (MODELS AND MODEL M)

K-Number: K961607 · 1996-12-06

Decision Date1996-12-06

Product CodeFEB

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

VIRAPUMP II (MODELS AND MODEL M) is the device name listed in this FDA 510(k) record. The listed applicant is Viatro, Corp.. It received FDA 510(k) clearance on 1996-12-06 under 510(k) number K961607. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRAPUMP II (MODELS AND MODEL M)?

VIRAPUMP II (MODELS AND MODEL M) is a medical device that received FDA 510(k) clearance on 1996-12-06. The listed applicant is Viatro, Corp.. The 510(k) number is K961607.

When did VIRAPUMP II (MODELS AND MODEL M) receive FDA 510(k) clearance?

VIRAPUMP II (MODELS AND MODEL M) received FDA 510(k) clearance on 1996-12-06, under 510(k) number K961607.

Who is the listed applicant for VIRAPUMP II (MODELS AND MODEL M)?

The FDA 510(k) record lists Viatro, Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRAPUMP II (MODELS AND MODEL M)?

The FDA product code for VIRAPUMP II (MODELS AND MODEL M) is FEB.

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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.