GRASPING TRIPOD FORCEP (MODEL 23/25)
K-Number: K874006 · 1987-12-29
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Device Summary
Frequently Asked Questions
What is the GRASPING TRIPOD FORCEP (MODEL 23/25)?
GRASPING TRIPOD FORCEP (MODEL 23/25) is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Endovations. The 510(k) number is K874006.
When did GRASPING TRIPOD FORCEP (MODEL 23/25) receive FDA 510(k) clearance?
GRASPING TRIPOD FORCEP (MODEL 23/25) received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874006.
Who is the listed applicant for GRASPING TRIPOD FORCEP (MODEL 23/25)?
The FDA 510(k) record lists Endovations as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRASPING TRIPOD FORCEP (MODEL 23/25)?
The FDA product code for GRASPING TRIPOD FORCEP (MODEL 23/25) 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 Endovations 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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