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FDA 510(k)

SURGICAL BLADE HANDLES

K-Number: K761035 · 1976-12-21

Decision Date1976-12-21
Product CodeGDZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL BLADE HANDLES 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 1976-12-21 under 510(k) number K761035. The device is classified under product code GDZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL BLADE HANDLES?

SURGICAL BLADE HANDLES is a medical device that received FDA 510(k) clearance on 1976-12-21. The listed applicant is Parke-Davis Co.. The 510(k) number is K761035.

When did SURGICAL BLADE HANDLES receive FDA 510(k) clearance?

SURGICAL BLADE HANDLES received FDA 510(k) clearance on 1976-12-21, under 510(k) number K761035.

Who is the listed applicant for SURGICAL BLADE HANDLES?

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

What is the FDA product code for SURGICAL BLADE HANDLES?

The FDA product code for SURGICAL BLADE HANDLES is GDZ.

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.

View all 47 devices →

Related Devices (Code: GDZ)

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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