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FDA 510(k)

SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT

K-Number: K872847 · 1987-08-10

ApplicantCandace Lane Corp.
Decision Date1987-08-10
Product CodeKIS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Candace Lane Corp.. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K872847. The device is classified under product code KIS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT?

SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Candace Lane Corp.. The 510(k) number is K872847.

When did SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT receive FDA 510(k) clearance?

SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT received FDA 510(k) clearance on 1987-08-10, under 510(k) number K872847.

Who is the listed applicant for SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT?

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

What is the FDA product code for SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT?

The FDA product code for SOLCOSERYL TISSUE CULTURE GROWTH SUPPLEMENT is KIS.

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Related Devices (Code: KIS)

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.

K881287ANIMAL AND HUMAN SERACell Culture LaboratoriesK880471BOVINE CALF SERUM SUPPLEMENTED #A-2159Hyclone Laboratories, Inc.K880470BOVINE CALF SERUM CATALOG #A-2119Hyclone Laboratories, Inc.K870580MLC NORMAL SERUMRjo Biologicals, Inc.K870938FETAL BOVINE SERUMHyclone Laboratories, Inc.K870466DEFINED CALF BOVINE SERUM #A-2111Hyclone Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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