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FDA 510(k)

WASHER SYSTEM, MICROELISA

K-Number: K781802 · 1978-12-20

ApplicantMetrix Teknika, Inc.
Decision Date1978-12-20
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

WASHER SYSTEM, MICROELISA is the device name listed in this FDA 510(k) record. The listed applicant is Metrix Teknika, Inc.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781802. 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 WASHER SYSTEM, MICROELISA?

WASHER SYSTEM, MICROELISA is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Metrix Teknika, Inc.. The 510(k) number is K781802.

When did WASHER SYSTEM, MICROELISA receive FDA 510(k) clearance?

WASHER SYSTEM, MICROELISA received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781802.

Who is the listed applicant for WASHER SYSTEM, MICROELISA?

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

What is the FDA product code for WASHER SYSTEM, MICROELISA?

The FDA product code for WASHER SYSTEM, MICROELISA is JTC.

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 Metrix Teknika, 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.

K781803FILTER, EYRPUR DISPOSABLE LEUKOCITEK781348FOCISCAN ECHOVISOR SYSTEMK780035MINIVISOR

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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