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FDA 510(k)

MICRO CARRIER

K-Number: K860783 · 1986-03-12

ApplicantTissue Culture Innovations
Decision Date1986-03-12
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MICRO CARRIER is the device name listed in this FDA 510(k) record. The listed applicant is Tissue Culture Innovations. It received FDA 510(k) clearance on 1986-03-12 under 510(k) number K860783. 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 MICRO CARRIER?

MICRO CARRIER is a medical device that received FDA 510(k) clearance on 1986-03-12. The listed applicant is Tissue Culture Innovations. The 510(k) number is K860783.

When did MICRO CARRIER receive FDA 510(k) clearance?

MICRO CARRIER received FDA 510(k) clearance on 1986-03-12, under 510(k) number K860783.

Who is the listed applicant for MICRO CARRIER?

The FDA 510(k) record lists Tissue Culture Innovations as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO CARRIER?

The FDA product code for MICRO CARRIER is KIT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Tissue Culture Innovations 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.

K860785HAM'S F-12 W/NAHCO3K860784DULBECCO'S PHOSPHATE BUFFERED SALINE W/CALCL2K860786RPMI 1640 HEPESK860787DULBECCO'S MEMK860788HAM'S F-12 W/GLUTAMINE & NAHCO3

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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