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FDA 510(k)

BIO-TEK AUTOMATED MICROPLATE WASHER EL402

K-Number: K850249 · 1985-03-13

ApplicantBio-Tek Instruments, Inc.
Decision Date1985-03-13
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BIO-TEK AUTOMATED MICROPLATE WASHER EL402 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Tek Instruments, Inc.. It received FDA 510(k) clearance on 1985-03-13 under 510(k) number K850249. 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 BIO-TEK AUTOMATED MICROPLATE WASHER EL402?

BIO-TEK AUTOMATED MICROPLATE WASHER EL402 is a medical device that received FDA 510(k) clearance on 1985-03-13. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K850249.

When did BIO-TEK AUTOMATED MICROPLATE WASHER EL402 receive FDA 510(k) clearance?

BIO-TEK AUTOMATED MICROPLATE WASHER EL402 received FDA 510(k) clearance on 1985-03-13, under 510(k) number K850249.

Who is the listed applicant for BIO-TEK AUTOMATED MICROPLATE WASHER EL402?

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

What is the FDA product code for BIO-TEK AUTOMATED MICROPLATE WASHER EL402?

The FDA product code for BIO-TEK AUTOMATED MICROPLATE WASHER EL402 is JTC.

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Other records listing Bio-Tek Instruments, 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.

K973609IDA-4 AND IPT-MCK971273INDEX 2E, INDEX 2F, INDEX 2EF, CARDIOSAT 100E, CARDIOSAT 100F, CARDIOSAT 100EFK961862MODELS IDA-2 PLUS AND IPT-1K954391MODELS QED-6, 6M AND 6H DEFIBRILLATOR ANALYZER WITH OPTIONAL UNIVERSAL PACEMAKER LOAD ADAPTERK953710ELX808 AUTOMATED MICROPLATE READERSK953572ELX800UV

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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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