SCISSOR'S #'S 2294,2262,2263
K-Number: K791984 · 1979-10-17
Advertisement
Device Summary
Frequently Asked Questions
What is the SCISSOR'S #'S 2294,2262,2263?
SCISSOR'S #'S 2294,2262,2263 is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791984.
When did SCISSOR'S #'S 2294,2262,2263 receive FDA 510(k) clearance?
SCISSOR'S #'S 2294,2262,2263 received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791984.
Who is the listed applicant for SCISSOR'S #'S 2294,2262,2263?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCISSOR'S #'S 2294,2262,2263?
The FDA product code for SCISSOR'S #'S 2294,2262,2263 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 Edward Weck, 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.
Advertisement