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FDA 510(k)

PIGGYBACK VENOSET W/0.22 FILTER

K-Number: K770518 · 1977-04-29

ApplicantAbbott Laboratories
Decision Date1977-04-29
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PIGGYBACK VENOSET W/0.22 FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1977-04-29 under 510(k) number K770518. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIGGYBACK VENOSET W/0.22 FILTER?

PIGGYBACK VENOSET W/0.22 FILTER is a medical device that received FDA 510(k) clearance on 1977-04-29. The listed applicant is Abbott Laboratories. The 510(k) number is K770518.

When did PIGGYBACK VENOSET W/0.22 FILTER receive FDA 510(k) clearance?

PIGGYBACK VENOSET W/0.22 FILTER received FDA 510(k) clearance on 1977-04-29, under 510(k) number K770518.

Who is the listed applicant for PIGGYBACK VENOSET W/0.22 FILTER?

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

What is the FDA product code for PIGGYBACK VENOSET W/0.22 FILTER?

The FDA product code for PIGGYBACK VENOSET W/0.22 FILTER is FPA.

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Related Devices (Code: FPA)

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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.

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