3 CHANNEL KNEE ELECTRONIC AMPLIFIED STETHOSCOPE
K-Number: K991756 · 1999-12-10
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Device Summary
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.
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
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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