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FDA 510(k)

ANTRUM & ATTIC MIRROR

K-Number: K833601 · 1984-01-03

Decision Date1984-01-03
Product CodeKAI
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ANTRUM & ATTIC MIRROR is the device name listed in this FDA 510(k) record. The listed applicant is Microtek Medical, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833601. 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 ANTRUM & ATTIC MIRROR?

ANTRUM & ATTIC MIRROR is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Microtek Medical, Inc.. The 510(k) number is K833601.

When did ANTRUM & ATTIC MIRROR receive FDA 510(k) clearance?

ANTRUM & ATTIC MIRROR received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833601.

Who is the listed applicant for ANTRUM & ATTIC MIRROR?

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

What is the FDA product code for ANTRUM & ATTIC MIRROR?

The FDA product code for ANTRUM & ATTIC MIRROR 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.

Other records listing Microtek Medical, 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 24 devices →

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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