SNAP OSCILLATING SAW
K-Number: K931769 · 1994-01-27
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Device Summary
Frequently Asked Questions
What is the SNAP OSCILLATING SAW?
SNAP OSCILLATING SAW 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 K931769.
When did SNAP OSCILLATING SAW receive FDA 510(k) clearance?
SNAP OSCILLATING SAW received FDA 510(k) clearance on 1994-01-27, under 510(k) number K931769.
Who is the listed applicant for SNAP OSCILLATING 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 OSCILLATING SAW?
The FDA product code for SNAP OSCILLATING SAW is GFA.
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: GFA)
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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