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FDA 510(k)

TEGTMEIER MAMMOMETER

K-Number: K791221 · 1979-07-03

ApplicantAztec Medical Products, Inc.
Decision Date1979-07-03
Product Code
DecisionUnknown

Device Summary

TEGTMEIER MAMMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Aztec Medical Products, Inc.. It received FDA 510(k) clearance on 1979-07-03 under 510(k) number K791221. FDA Decision: Unknown.

Frequently Asked Questions

What is the TEGTMEIER MAMMOMETER?

TEGTMEIER MAMMOMETER is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Aztec Medical Products, Inc.. The 510(k) number is K791221.

When did TEGTMEIER MAMMOMETER receive FDA 510(k) clearance?

TEGTMEIER MAMMOMETER received FDA 510(k) clearance on 1979-07-03, under 510(k) number K791221.

Who is the listed applicant for TEGTMEIER MAMMOMETER?

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

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Other records listing Aztec Medical Products, 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.

K801939RHYTIDOMETERK801937BLEPHAROMETERK801938RHINOMETERK792608TEGTMEIER MAMMOMETER

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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