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FDA 510(k)

SNAP DRILL

K-Number: K935516 · 1994-01-27

Decision Date1994-01-27
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SNAP DRILL is the device name listed in this FDA 510(k) record. The listed applicant is Surgiquip, Inc.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K935516. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAP DRILL?

SNAP DRILL is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Surgiquip, Inc.. The 510(k) number is K935516.

When did SNAP DRILL receive FDA 510(k) clearance?

SNAP DRILL received FDA 510(k) clearance on 1994-01-27, under 510(k) number K935516.

Who is the listed applicant for SNAP DRILL?

The FDA 510(k) record lists Surgiquip, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNAP DRILL?

The FDA product code for SNAP DRILL is HWE.

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 Surgiquip, Inc. 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: HWE)

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

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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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