COMPOUND LEVERAGE SNIP
K-Number: K861952 · 1986-06-06
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Device Summary
Frequently Asked Questions
What is the COMPOUND LEVERAGE SNIP?
COMPOUND LEVERAGE SNIP is a medical device that received FDA 510(k) clearance on 1986-06-06. The listed applicant is Med-Tool, Inc.. The 510(k) number is K861952.
When did COMPOUND LEVERAGE SNIP receive FDA 510(k) clearance?
COMPOUND LEVERAGE SNIP received FDA 510(k) clearance on 1986-06-06, under 510(k) number K861952.
Who is the listed applicant for COMPOUND LEVERAGE SNIP?
The FDA 510(k) record lists Med-Tool, Inc. as the applicant. This does not by itself establish the device manufacturer.
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 Med-Tool, 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.
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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