BOWEN PROBE
K-Number: K863149 · 1986-09-05
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Device Summary
Frequently Asked Questions
What is the BOWEN PROBE?
BOWEN PROBE is a medical device that received FDA 510(k) clearance on 1986-09-05. The listed applicant is Bowen & Company, Inc.. The 510(k) number is K863149.
When did BOWEN PROBE receive FDA 510(k) clearance?
BOWEN PROBE received FDA 510(k) clearance on 1986-09-05, under 510(k) number K863149.
Who is the listed applicant for BOWEN PROBE?
The FDA 510(k) record lists Bowen & Company, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOWEN PROBE?
The FDA product code for BOWEN PROBE is HXB.
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 Bowen & Company, 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: HXB)
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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