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FDA 510(k)

ATMOS MIRROR WARMER

K-Number: K920988 · 1992-05-15

Decision Date1992-05-15
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ATMOS MIRROR WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1992-05-15 under 510(k) number K920988. The device is classified under product code LRC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATMOS MIRROR WARMER?

ATMOS MIRROR WARMER is a medical device that received FDA 510(k) clearance on 1992-05-15. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K920988.

When did ATMOS MIRROR WARMER receive FDA 510(k) clearance?

ATMOS MIRROR WARMER received FDA 510(k) clearance on 1992-05-15, under 510(k) number K920988.

Who is the listed applicant for ATMOS MIRROR WARMER?

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

What is the FDA product code for ATMOS MIRROR WARMER?

The FDA product code for ATMOS MIRROR WARMER is LRC.

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 Jedmed Instrument Co. 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 91 devices →

Related Devices (Code: LRC)

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

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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