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FDA 510(k)

STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE

K-Number: K854356 · 1986-05-05

ApplicantFontaine Industries, Inc.
Decision Date1986-05-05
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE is the device name listed in this FDA 510(k) record. The listed applicant is Fontaine Industries, Inc.. It received FDA 510(k) clearance on 1986-05-05 under 510(k) number K854356. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE?

STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE is a medical device that received FDA 510(k) clearance on 1986-05-05. The listed applicant is Fontaine Industries, Inc.. The 510(k) number is K854356.

When did STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE receive FDA 510(k) clearance?

STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE received FDA 510(k) clearance on 1986-05-05, under 510(k) number K854356.

Who is the listed applicant for STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE?

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

What is the FDA product code for STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE?

The FDA product code for STETHOSCOPE ELECTRONIC STETHOSCOPE SPHYGMOMANOMETE is DQD.

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Related Devices (Code: DQD)

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.

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Official Source

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