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FDA 510(k)

CONPHAR WALL MODEL MERCURY SPHYGMOMAN.

K-Number: K801182 · 1980-06-04

ApplicantConphar, Inc.
Decision Date1980-06-04
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONPHAR WALL MODEL MERCURY SPHYGMOMAN. is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1980-06-04 under 510(k) number K801182. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR WALL MODEL MERCURY SPHYGMOMAN.?

CONPHAR WALL MODEL MERCURY SPHYGMOMAN. is a medical device that received FDA 510(k) clearance on 1980-06-04. The listed applicant is Conphar, Inc.. The 510(k) number is K801182.

When did CONPHAR WALL MODEL MERCURY SPHYGMOMAN. receive FDA 510(k) clearance?

CONPHAR WALL MODEL MERCURY SPHYGMOMAN. received FDA 510(k) clearance on 1980-06-04, under 510(k) number K801182.

Who is the listed applicant for CONPHAR WALL MODEL MERCURY SPHYGMOMAN.?

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

What is the FDA product code for CONPHAR WALL MODEL MERCURY SPHYGMOMAN.?

The FDA product code for CONPHAR WALL MODEL MERCURY SPHYGMOMAN. is DXQ.

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Related Devices (Code: DXQ)

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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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