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FDA 510(k)

GIT SERUM-FREE MEDIUM FOR CELL CULTURE

K-Number: K872918 · 1987-08-11

ApplicantWako Chemicals USA, Inc.
Decision Date1987-08-11
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

GIT SERUM-FREE MEDIUM FOR CELL CULTURE is the device name listed in this FDA 510(k) record. The listed applicant is Wako Chemicals USA, Inc.. It received FDA 510(k) clearance on 1987-08-11 under 510(k) number K872918. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIT SERUM-FREE MEDIUM FOR CELL CULTURE?

GIT SERUM-FREE MEDIUM FOR CELL CULTURE is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is Wako Chemicals USA, Inc.. The 510(k) number is K872918.

When did GIT SERUM-FREE MEDIUM FOR CELL CULTURE receive FDA 510(k) clearance?

GIT SERUM-FREE MEDIUM FOR CELL CULTURE received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872918.

Who is the listed applicant for GIT SERUM-FREE MEDIUM FOR CELL CULTURE?

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

What is the FDA product code for GIT SERUM-FREE MEDIUM FOR CELL CULTURE?

The FDA product code for GIT SERUM-FREE MEDIUM FOR CELL CULTURE is KIT.

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Other records listing Wako Chemicals USA, 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.

K100464UTASWAKO I30 (INCLUDES ACCESSORIES), UTASWAKO AFP-L3, CALIBRATOR SET, CONTROL L, CONTROL H, SAMPLE DILUTIONK080125APOLOWAKO T-CHO, HDL-C, TG AND ANALYZER, MODELS 993-23501, 999-23601, 995-23701 AND 993-25201K080123APOLOWAKO HBA1C, GLUCOSE AND ANALYZER, MODELS 993-24601, 991-24401 AND 993-25201K061775WAKO L-TYPE CREATININE-M TEST, AND WAKO CREATININE CALIBRATORK062368WAKO LBA DCP TEST SYSTEM, MODEL 993-05301; DCP CONTROL SET, MODEL 995-0551; DCP CALIBRATOR SET, LIBASYS, MODEL 999-05401K053131WAKO TOTAL BILIRUBIN V, MODELS 410-22701, 998-23291, 416-22801, 990-23191

View all 123 devices →

Related Devices (Code: KIT)

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.

K892938AMNIO-GROW TMInovar Biologicals, Inc.K890700MELANOCYTE GROWTH MEDIUM (MGM)Clonetics Corp.K890701ENDOTHELIAL GROWTH MEDIUM (EGM)Clonetics Corp.K890482ABC, ABC-1X, ABC(TM)Cell Ent., Inc.K884654ALPHACALF SERUMHyclone Laboratories, Inc.K884572RPMI-1640 HYBRI-MAX, PROD. NO. R5382Sigma Chemical Co.

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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