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FDA 510(k)

CHARGED SUPOR(R) FILTER EXTENSION SET

K-Number: K940980 · 1994-07-14

ApplicantB. Braun of America, Inc.
Decision Date1994-07-14
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHARGED SUPOR(R) FILTER EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun of America, Inc.. It received FDA 510(k) clearance on 1994-07-14 under 510(k) number K940980. 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 CHARGED SUPOR(R) FILTER EXTENSION SET?

CHARGED SUPOR(R) FILTER EXTENSION SET is a medical device that received FDA 510(k) clearance on 1994-07-14. The listed applicant is B. Braun of America, Inc.. The 510(k) number is K940980.

When did CHARGED SUPOR(R) FILTER EXTENSION SET receive FDA 510(k) clearance?

CHARGED SUPOR(R) FILTER EXTENSION SET received FDA 510(k) clearance on 1994-07-14, under 510(k) number K940980.

Who is the listed applicant for CHARGED SUPOR(R) FILTER EXTENSION SET?

The FDA 510(k) record lists B. Braun of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHARGED SUPOR(R) FILTER EXTENSION SET?

The FDA product code for CHARGED SUPOR(R) FILTER EXTENSION SET is FPB.

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Other records listing B. Braun of America, Inc. as applicant

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.

K993024CELSITE IMPLANTABLE PORT WITH VALVED CATHETERK983794CHEMO MINI SPIKE PLUSK946170COMFORT-Q SUBCUTANEOUS INJECTION SETSK945850BRAUN DIACAN(R) FISTULA NEEDLESK942988FILTERED EXTENSION SETSK945752CELSITE(TM) BRACHIAL VENOUS PORT

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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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