BIOSPSY FORCEPS
K-Number: K920762 · 1992-08-26
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Device Summary
Frequently Asked Questions
What is the BIOSPSY FORCEPS?
BIOSPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1992-08-26. The listed applicant is Symbiosis Corp.. The 510(k) number is K920762.
When did BIOSPSY FORCEPS receive FDA 510(k) clearance?
BIOSPSY FORCEPS received FDA 510(k) clearance on 1992-08-26, under 510(k) number K920762.
Who is the listed applicant for BIOSPSY FORCEPS?
The FDA 510(k) record lists Symbiosis Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOSPSY FORCEPS?
The FDA product code for BIOSPSY FORCEPS is OCZ.
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 Symbiosis Corp. 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: OCZ)
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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