BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE
K-Number: K875119 · 1988-03-02
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Device Summary
Frequently Asked Questions
What is the BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE?
BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE is a medical device that received FDA 510(k) clearance on 1988-03-02. The listed applicant is Advanced Diagnostic Medical Systems, Inc.. The 510(k) number is K875119.
When did BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE receive FDA 510(k) clearance?
BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE received FDA 510(k) clearance on 1988-03-02, under 510(k) number K875119.
Who is the listed applicant for BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE?
The FDA 510(k) record lists Advanced Diagnostic Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE?
The FDA product code for BIOPSY ATTACH. FOR ADMS ULTRASOUND PROBE is FCI.
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 Advanced Diagnostic Medical Systems, 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: FCI)
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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