BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL
K-Number: K873673 · 1988-02-26
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Device Summary
Frequently Asked Questions
What is the BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL?
BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Sonicaid, Inc.. The 510(k) number is K873673.
When did BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL receive FDA 510(k) clearance?
BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL received FDA 510(k) clearance on 1988-02-26, under 510(k) number K873673.
Who is the listed applicant for BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL?
The FDA 510(k) record lists Sonicaid, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL?
The FDA product code for BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL is DPT.
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 Sonicaid, 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: DPT)
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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