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FDA 510(k)

PRIMARY PIGGYBACK VENOSET W/ FILTER

K-Number: K771594 · 1977-09-28

ApplicantAbbott Laboratories
Decision Date1977-09-28
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRIMARY PIGGYBACK VENOSET W/ 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 1977-09-28 under 510(k) number K771594. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRIMARY PIGGYBACK VENOSET W/ FILTER?

PRIMARY PIGGYBACK VENOSET W/ FILTER is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Abbott Laboratories. The 510(k) number is K771594.

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

PRIMARY PIGGYBACK VENOSET W/ FILTER received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771594.

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

The FDA product code for PRIMARY PIGGYBACK VENOSET W/ FILTER is FPB.

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Related Devices (Code: FPB)

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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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