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FDA 510(k)

TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA

K-Number: K850908 · 1985-03-25

ApplicantFlow Laboratories, Inc.
Decision Date1985-03-25
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1985-03-25 under 510(k) number K850908. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA?

TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA is a medical device that received FDA 510(k) clearance on 1985-03-25. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K850908.

When did TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA receive FDA 510(k) clearance?

TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA received FDA 510(k) clearance on 1985-03-25, under 510(k) number K850908.

Who is the listed applicant for TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA?

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

What is the FDA product code for TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA?

The FDA product code for TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA is JTC.

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Other records listing Flow Laboratories, 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.

K861897UNISKAN IIK862066TITERTEK MICROPLATE WASHER S-12K861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)K861823GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEK860762GAMMA-FREE HORSE SERUM

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Related Devices (Code: JTC)

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.

K924907FILTERMATE UNIVERSAL HARVESTERPackard Instrument Co., Inc.K901808MICROMATE 196 MODEL A961960Packard Instrument Co., Inc.K894645IMMULON 1,2,3,AND 4 DIVIDASTRIPS TMDynatech Laboratories, Inc.K892369MULTI-PROBE HEAD PLUSHamilton Co.K891766GENETIC SYSTEMS MICROPLATE STRIP WASHERGenetic Systems Corp.K891765GENETIC SYSTEMS PIPETTOR/DILUTORGenetic Systems Corp.

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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