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FDA 510(k)

MIRROR WARMER

K-Number: K781750 · 1979-01-17

Decision Date1979-01-17
Product CodeKAI
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MIRROR WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Arleton Technical Products, Inc.. It received FDA 510(k) clearance on 1979-01-17 under 510(k) number K781750. The device is classified under product code KAI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIRROR WARMER?

MIRROR WARMER is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Arleton Technical Products, Inc.. The 510(k) number is K781750.

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

MIRROR WARMER received FDA 510(k) clearance on 1979-01-17, under 510(k) number K781750.

Who is the listed applicant for MIRROR WARMER?

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

What is the FDA product code for MIRROR WARMER?

The FDA product code for MIRROR WARMER is KAI.

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.

Related Devices (Code: KAI)

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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