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FDA 510(k)

3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE

K-Number: K991756 · 1999-12-10

Decision Date1999-12-10
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Research Associates, Inc.. It received FDA 510(k) clearance on 1999-12-10 under 510(k) number K991756. 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 3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE?

3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1999-12-10. The listed applicant is Bio-Research Associates, Inc.. The 510(k) number is K991756.

When did 3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE receive FDA 510(k) clearance?

3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE received FDA 510(k) clearance on 1999-12-10, under 510(k) number K991756.

Who is the listed applicant for 3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE?

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

What is the FDA product code for 3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE?

The FDA product code for 3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE is DQD.

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 Bio-Research Associates, 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.

View all 10 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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