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FDA 510(k)

AUTOPRIME

K-Number: K964283 · 1997-01-22

ApplicantArbor Technologies, Inc.
Decision Date1997-01-22
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTOPRIME is the device name listed in this FDA 510(k) record. The listed applicant is Arbor Technologies, Inc.. It received FDA 510(k) clearance on 1997-01-22 under 510(k) number K964283. 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 AUTOPRIME?

AUTOPRIME is a medical device that received FDA 510(k) clearance on 1997-01-22. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K964283.

When did AUTOPRIME receive FDA 510(k) clearance?

AUTOPRIME received FDA 510(k) clearance on 1997-01-22, under 510(k) number K964283.

Who is the listed applicant for AUTOPRIME?

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

What is the FDA product code for AUTOPRIME?

The FDA product code for AUTOPRIME is FPB.

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Other records listing Arbor Technologies, 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.

K960928SYRINGEFILTERK922777PRESSURE TUBING AND ACCESSORIESK902666ANESTHESIA CONDUCTION FILTERK895859CONTAIN(TM)K902167CONTAIN(TM) LASER PLUME FILTERK890844MICROSEPT 60/20

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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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