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FDA 510(k)

RHINOMETER

K-Number: K801938 · 1980-09-09

ApplicantAztec Medical Products, Inc.
Decision Date1980-09-09
Product CodeJYJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RHINOMETER 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 1980-09-09 under 510(k) number K801938. The device is classified under product code JYJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHINOMETER?

RHINOMETER is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Aztec Medical Products, Inc.. The 510(k) number is K801938.

When did RHINOMETER receive FDA 510(k) clearance?

RHINOMETER received FDA 510(k) clearance on 1980-09-09, under 510(k) number K801938.

Who is the listed applicant for RHINOMETER?

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

What is the FDA product code for RHINOMETER?

The FDA product code for RHINOMETER is JYJ.

Related Clinical Trials

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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.

K801939RHYTIDOMETERK801937BLEPHAROMETERK792608TEGTMEIER MAMMOMETERK791221TEGTMEIER MAMMOMETER

Related Devices (Code: JYJ)

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.

K904469EYEOPENERKc Medical IndustriesK884974ACCESSORY TO EYEDROP GUIDESuredrop, Inc.K874569SUREDROP EYEDROP GUIDESuredrop, Inc.K833606IMPLANT MEASURING GAUGEMicrotek Medical, Inc.

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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