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FDA 510(k)

FILTERSET W/Y-INJECTION SITE, 0.2

K-Number: K772312 · 1978-01-26

ApplicantAbbott Laboratories
Decision Date1978-01-26
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FILTERSET W/Y-INJECTION SITE, 0.2 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K772312. 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 FILTERSET W/Y-INJECTION SITE, 0.2?

FILTERSET W/Y-INJECTION SITE, 0.2 is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Abbott Laboratories. The 510(k) number is K772312.

When did FILTERSET W/Y-INJECTION SITE, 0.2 receive FDA 510(k) clearance?

FILTERSET W/Y-INJECTION SITE, 0.2 received FDA 510(k) clearance on 1978-01-26, under 510(k) number K772312.

Who is the listed applicant for FILTERSET W/Y-INJECTION SITE, 0.2?

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 FILTERSET W/Y-INJECTION SITE, 0.2?

The FDA product code for FILTERSET W/Y-INJECTION SITE, 0.2 is FPB.

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Related Devices (Code: FPB)

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.

K261403Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion FilterGlobal Life Sciences Solutions USA, LLCK233277Filter Needle for Single UseHangzhou Qiantang Longyue Biotechnology Co., Ltd.K113227NON-DEHP MICRO-VOLUME EXTENSION SET WITH 0.22 MICRON FILTERBaxter Healthcare CorpK021293ARTERIA BLOOD FILTERArteria Medical Science, Inc.K993379PALL SUPOR AEF FILTERPall Corp.K9746610.2 U BACTERIAL FILTERSims Deltec, Inc.

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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