THOREK SCISSORS 7 1/4 & 10
K-Number: K771806 · 1977-10-04
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Device Summary
Frequently Asked Questions
What is the THOREK SCISSORS 7 1/4 & 10?
THOREK SCISSORS 7 1/4 & 10 is a medical device that received FDA 510(k) clearance on 1977-10-04. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K771806.
When did THOREK SCISSORS 7 1/4 & 10 receive FDA 510(k) clearance?
THOREK SCISSORS 7 1/4 & 10 received FDA 510(k) clearance on 1977-10-04, under 510(k) number K771806.
Who is the listed applicant for THOREK SCISSORS 7 1/4 & 10?
The FDA 510(k) record lists J. Sklar Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THOREK SCISSORS 7 1/4 & 10?
The FDA product code for THOREK SCISSORS 7 1/4 & 10 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 J. Sklar Mfg. 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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