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FDA 510(k)

SURGICAL MICRO DRILL

K-Number: K760956 · 1976-11-19

Decision Date1976-11-19
Product CodeDZA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SURGICAL MICRO DRILL is the device name listed in this FDA 510(k) record. The listed applicant is American Safety Equipment Corp.. It received FDA 510(k) clearance on 1976-11-19 under 510(k) number K760956. The device is classified under product code DZA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL MICRO DRILL?

SURGICAL MICRO DRILL is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is American Safety Equipment Corp.. The 510(k) number is K760956.

When did SURGICAL MICRO DRILL receive FDA 510(k) clearance?

SURGICAL MICRO DRILL received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760956.

Who is the listed applicant for SURGICAL MICRO DRILL?

The FDA 510(k) record lists American Safety Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL MICRO DRILL?

The FDA product code for SURGICAL MICRO DRILL is DZA.

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 American Safety Equipment 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.

View all 7 devices →

Related Devices (Code: DZA)

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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