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FDA 510(k)

SNAP RECIPROCATING SAW

K-Number: K935357 · 1994-01-28

Decision Date1994-01-28
Product CodeGAF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SNAP RECIPROCATING SAW is the device name listed in this FDA 510(k) record. The listed applicant is Surgiquip, Inc.. It received FDA 510(k) clearance on 1994-01-28 under 510(k) number K935357. The device is classified under product code GAF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAP RECIPROCATING SAW?

SNAP RECIPROCATING SAW is a medical device that received FDA 510(k) clearance on 1994-01-28. The listed applicant is Surgiquip, Inc.. The 510(k) number is K935357.

When did SNAP RECIPROCATING SAW receive FDA 510(k) clearance?

SNAP RECIPROCATING SAW received FDA 510(k) clearance on 1994-01-28, under 510(k) number K935357.

Who is the listed applicant for SNAP RECIPROCATING SAW?

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 RECIPROCATING SAW?

The FDA product code for SNAP RECIPROCATING SAW is GAF.

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: GAF)

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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