HACKSAW
K-Number: K864018 · 1986-10-30
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Device Summary
Frequently Asked Questions
What is the HACKSAW?
HACKSAW is a medical device that received FDA 510(k) clearance on 1986-10-30. The listed applicant is Med-Tool, Inc.. The 510(k) number is K864018.
When did HACKSAW receive FDA 510(k) clearance?
HACKSAW received FDA 510(k) clearance on 1986-10-30, under 510(k) number K864018.
Who is the listed applicant for HACKSAW?
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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