BIODYNAMICS FEMORAL CANAL BRUSH #1201
K-Number: K870349 · 1987-02-13
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Device Summary
Frequently Asked Questions
What is the BIODYNAMICS FEMORAL CANAL BRUSH #1201?
BIODYNAMICS FEMORAL CANAL BRUSH #1201 is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K870349.
When did BIODYNAMICS FEMORAL CANAL BRUSH #1201 receive FDA 510(k) clearance?
BIODYNAMICS FEMORAL CANAL BRUSH #1201 received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870349.
Who is the listed applicant for BIODYNAMICS FEMORAL CANAL BRUSH #1201?
The FDA 510(k) record lists Biodynamic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIODYNAMICS FEMORAL CANAL BRUSH #1201?
The FDA product code for BIODYNAMICS FEMORAL CANAL BRUSH #1201 is HTR.
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 Biodynamic Technologies, 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: HTR)
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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