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FDA 510(k)

STAR

K-Number: K810873 · 1981-04-23

Decision Date1981-04-23
Product CodeJWM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STAR is the device name listed in this FDA 510(k) record. The listed applicant is Intl. General Electric Co.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810873. The device is classified under product code JWM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAR?

STAR is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Intl. General Electric Co.. The 510(k) number is K810873.

When did STAR receive FDA 510(k) clearance?

STAR received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810873.

Who is the listed applicant for STAR?

The FDA 510(k) record lists Intl. General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAR?

The FDA product code for STAR is JWM.

Related PubMed Literature

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.

Related Devices (Code: JWM)

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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