ANTRUM & ATTIC MIRROR
K-Number: K833601 · 1984-01-03
Advertisement
Device Summary
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.
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.
Advertisement