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FDA 510(k)

CULTURE MEDIA FOR IN VITRO DIAG. USE

K-Number: K802892 · 1980-12-11

Decision Date1980-12-11
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CULTURE MEDIA FOR IN VITRO DIAG. USE is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Technology, Inc.. It received FDA 510(k) clearance on 1980-12-11 under 510(k) number K802892. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CULTURE MEDIA FOR IN VITRO DIAG. USE?

CULTURE MEDIA FOR IN VITRO DIAG. USE is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Radiation Technology, Inc.. The 510(k) number is K802892.

When did CULTURE MEDIA FOR IN VITRO DIAG. USE receive FDA 510(k) clearance?

CULTURE MEDIA FOR IN VITRO DIAG. USE received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802892.

Who is the listed applicant for CULTURE MEDIA FOR IN VITRO DIAG. USE?

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

What is the FDA product code for CULTURE MEDIA FOR IN VITRO DIAG. USE?

The FDA product code for CULTURE MEDIA FOR IN VITRO DIAG. USE is JSG.

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.

Other records listing Radiation Technology, 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.

View all 7 devices →

Related Devices (Code: JSG)

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.

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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