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FDA 510(k)

PEDIATRIC IV WATCH

K-Number: K852030 · 1985-05-30

ApplicantAlltek, Inc.
Decision Date1985-05-30
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC IV WATCH is the device name listed in this FDA 510(k) record. The listed applicant is Alltek, Inc.. It received FDA 510(k) clearance on 1985-05-30 under 510(k) number K852030. 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 PEDIATRIC IV WATCH?

PEDIATRIC IV WATCH is a medical device that received FDA 510(k) clearance on 1985-05-30. The listed applicant is Alltek, Inc.. The 510(k) number is K852030.

When did PEDIATRIC IV WATCH receive FDA 510(k) clearance?

PEDIATRIC IV WATCH received FDA 510(k) clearance on 1985-05-30, under 510(k) number K852030.

Who is the listed applicant for PEDIATRIC IV WATCH?

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

What is the FDA product code for PEDIATRIC IV WATCH?

The FDA product code for PEDIATRIC IV WATCH is FPB.

Related Clinical Trials

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.

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Other records listing Alltek, 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.

K854172I.V. WATCHK852029I.V. WATCHK840495MANUAL IRRIGATING/ASPIRATING UNITK834376FILTRARE TM ALLVENT TM

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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