RAT TOOTH GRASPING FORCEP (MODEL 23/20)
K-Number: K874005 · 1987-12-29
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Device Summary
Frequently Asked Questions
What is the RAT TOOTH GRASPING FORCEP (MODEL 23/20)?
RAT TOOTH GRASPING FORCEP (MODEL 23/20) is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Endovations. The 510(k) number is K874005.
When did RAT TOOTH GRASPING FORCEP (MODEL 23/20) receive FDA 510(k) clearance?
RAT TOOTH GRASPING FORCEP (MODEL 23/20) received FDA 510(k) clearance on 1987-12-29, under 510(k) number K874005.
Who is the listed applicant for RAT TOOTH GRASPING FORCEP (MODEL 23/20)?
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 RAT TOOTH GRASPING FORCEP (MODEL 23/20)?
The FDA product code for RAT TOOTH GRASPING FORCEP (MODEL 23/20) 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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