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FDA 510(k)

HL-1, DEFINED SERUM FREE MEDIA

K-Number: K841993 · 1984-06-25

ApplicantVentrex Laboratories, Inc.
Decision Date1984-06-25
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HL-1, DEFINED SERUM FREE MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-25 under 510(k) number K841993. 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 HL-1, DEFINED SERUM FREE MEDIA?

HL-1, DEFINED SERUM FREE MEDIA is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K841993.

When did HL-1, DEFINED SERUM FREE MEDIA receive FDA 510(k) clearance?

HL-1, DEFINED SERUM FREE MEDIA received FDA 510(k) clearance on 1984-06-25, under 510(k) number K841993.

Who is the listed applicant for HL-1, DEFINED SERUM FREE MEDIA?

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

What is the FDA product code for HL-1, DEFINED SERUM FREE MEDIA?

The FDA product code for HL-1, DEFINED SERUM FREE MEDIA is KIT.

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Other records listing Ventrex Laboratories, 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.

K914554SPECIFIC IGE EIA-TURBO ASSAYK913833VENTREX ALLERGEN DISCK913434VENTREX COATED TUBE INTACT PTHK905612VENTREX COATED TUBE IGE RADIOIMMUNOASSAYK905636VENTREX COATED TUBE IGE ENZYME IMMUNOASSAYK905247SHBG IRMA KIT

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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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