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FDA 510(k)

SURGICAL BLADES (BEAVER)

K-Number: K760016 · 1976-07-16

Decision Date1976-07-16
Product Code
DecisionSubstantially Equivalent

Device Summary

SURGICAL BLADES (BEAVER) is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760016. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL BLADES (BEAVER)?

SURGICAL BLADES (BEAVER) is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Parke-Davis Co.. The 510(k) number is K760016.

When did SURGICAL BLADES (BEAVER) receive FDA 510(k) clearance?

SURGICAL BLADES (BEAVER) received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760016.

Who is the listed applicant for SURGICAL BLADES (BEAVER)?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

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 Parke-Davis Co. 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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