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FDA 510(k)

BONE MARROW COLLECTION MEDIUM

K-Number: K864740 · 1987-01-05

ApplicantBioclinical Laboratory Services, Inc.
Decision Date1987-01-05
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BONE MARROW COLLECTION MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Bioclinical Laboratory Services, Inc.. It received FDA 510(k) clearance on 1987-01-05 under 510(k) number K864740. 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 BONE MARROW COLLECTION MEDIUM?

BONE MARROW COLLECTION MEDIUM is a medical device that received FDA 510(k) clearance on 1987-01-05. The listed applicant is Bioclinical Laboratory Services, Inc.. The 510(k) number is K864740.

When did BONE MARROW COLLECTION MEDIUM receive FDA 510(k) clearance?

BONE MARROW COLLECTION MEDIUM received FDA 510(k) clearance on 1987-01-05, under 510(k) number K864740.

Who is the listed applicant for BONE MARROW COLLECTION MEDIUM?

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

What is the FDA product code for BONE MARROW COLLECTION MEDIUM?

The FDA product code for BONE MARROW COLLECTION MEDIUM is KIT.

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Other records listing Bioclinical Laboratory Services, 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.

K870451SKIN GRAFT PRESERVATION MEDIUM (TISSUE)K870249MCCAREY-KAUFMAN CORNEAL STORAGE MEDIUMK870251CHONDROITIN SULFATE CORNEAL STORAGE MEDIUMK870250MODIFIED MCCAREY-KAUFMAN CORNEAL STORAGE MEDIUMK864396LYMPHOCYTE MAINTENANCE MEDIUM

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

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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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