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FDA 510(k)

SEROCLUSTER FLEXIBLE VINYL U & V PL.

K-Number: K803243 · 1981-01-28

ApplicantCorning Costar Corp.
Decision Date1981-01-28
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SEROCLUSTER FLEXIBLE VINYL U & V PL. is the device name listed in this FDA 510(k) record. The listed applicant is Corning Costar Corp.. It received FDA 510(k) clearance on 1981-01-28 under 510(k) number K803243. 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 SEROCLUSTER FLEXIBLE VINYL U & V PL.?

SEROCLUSTER FLEXIBLE VINYL U & V PL. is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is Corning Costar Corp.. The 510(k) number is K803243.

When did SEROCLUSTER FLEXIBLE VINYL U & V PL. receive FDA 510(k) clearance?

SEROCLUSTER FLEXIBLE VINYL U & V PL. received FDA 510(k) clearance on 1981-01-28, under 510(k) number K803243.

Who is the listed applicant for SEROCLUSTER FLEXIBLE VINYL U & V PL.?

The FDA 510(k) record lists Corning Costar Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEROCLUSTER FLEXIBLE VINYL U & V PL.?

The FDA product code for SEROCLUSTER FLEXIBLE VINYL U & V PL. is JTC.

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Other records listing Corning Costar Corp. 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.

K871559CELL LIFTERK860703U - STAR (MICRO-STAR)K823137OCTAPETTESK823138CELL SCRAPERK803244ASSAY STRIPSK803242SEROCLUSTER EIA PLATES

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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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