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FDA 510(k)

CELL SCRAPER

K-Number: K823138 · 1982-11-29

ApplicantCorning Costar Corp.
Decision Date1982-11-29
Product CodeKJA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CELL SCRAPER 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 1982-11-29 under 510(k) number K823138. The device is classified under product code KJA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CELL SCRAPER?

CELL SCRAPER is a medical device that received FDA 510(k) clearance on 1982-11-29. The listed applicant is Corning Costar Corp.. The 510(k) number is K823138.

When did CELL SCRAPER receive FDA 510(k) clearance?

CELL SCRAPER received FDA 510(k) clearance on 1982-11-29, under 510(k) number K823138.

Who is the listed applicant for CELL SCRAPER?

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 CELL SCRAPER?

The FDA product code for CELL SCRAPER is KJA.

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 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)K823137OCTAPETTESK803244ASSAY STRIPSK803242SEROCLUSTER EIA PLATESK803243SEROCLUSTER FLEXIBLE VINYL U & V PL.

View all 8 devices →

Related Devices (Code: KJA)

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.

K972404VACUTAINER BRAND SAFETY BLOOD COLLECTION ASSEMBLY(MULTIPLE)Bd Becton Dickinson Vacutainer Systems PreanalyticK933228KAPTON PEEL POUCHAmerican Fluoroseal Corp.K885121CELL SCRAPERBd Becton Dickinson Vacutainer Systems PreanalyticK873890TISSUE CULTURE FLASKSNunc, Inc.K873889TISSUE CULTURE TUBESNunc, Inc.K871324DU PONT STERICELL CELL CULTURE SYSTEME.I. Dupont DE Nemours & Co., Inc.

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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