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FDA 510(k)

SARTORIUS MINI-SART FH 16555

K-Number: K851817 · 1985-08-19

ApplicantSartorius Filters, Inc.
Decision Date1985-08-19
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SARTORIUS MINI-SART FH 16555 is the device name listed in this FDA 510(k) record. The listed applicant is Sartorius Filters, Inc.. It received FDA 510(k) clearance on 1985-08-19 under 510(k) number K851817. 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 SARTORIUS MINI-SART FH 16555?

SARTORIUS MINI-SART FH 16555 is a medical device that received FDA 510(k) clearance on 1985-08-19. The listed applicant is Sartorius Filters, Inc.. The 510(k) number is K851817.

When did SARTORIUS MINI-SART FH 16555 receive FDA 510(k) clearance?

SARTORIUS MINI-SART FH 16555 received FDA 510(k) clearance on 1985-08-19, under 510(k) number K851817.

Who is the listed applicant for SARTORIUS MINI-SART FH 16555?

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

What is the FDA product code for SARTORIUS MINI-SART FH 16555?

The FDA product code for SARTORIUS MINI-SART FH 16555 is FPB.

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Other records listing Sartorius Filters, 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.

K851818SARTORIUS MINI SART FH 16592K851816SARTORIUS MINISART FH 16534K850435SARTORIUS AQUASART SM 40035 - DIALYSATE SYSK844504SARTORIUS MINISART SM 16596HYK830487HEMO-PROCESSING SYSTEMK823132SARTOPHOR SYSTEM FOR ELECTROPHORESIS

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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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