SURGICAL STITCH CUTTER
K-Number: K800103 · 1980-01-28
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Device Summary
Frequently Asked Questions
What is the SURGICAL STITCH CUTTER?
SURGICAL STITCH CUTTER is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Macon & Co., Inc.. The 510(k) number is K800103.
When did SURGICAL STITCH CUTTER receive FDA 510(k) clearance?
SURGICAL STITCH CUTTER received FDA 510(k) clearance on 1980-01-28, under 510(k) number K800103.
Who is the listed applicant for SURGICAL STITCH CUTTER?
The FDA 510(k) record lists Macon & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGICAL STITCH CUTTER?
The FDA product code for SURGICAL STITCH CUTTER is FZT.
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 Macon & Co., 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: FZT)
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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