SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM.
K-Number: K770542 · 1977-04-15
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Device Summary
Frequently Asked Questions
What is the SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM.?
SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM. is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Sea-Pac Trading Corp.. The 510(k) number is K770542.
When did SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM. receive FDA 510(k) clearance?
SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM. received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770542.
Who is the listed applicant for SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM.?
The FDA 510(k) record lists Sea-Pac Trading Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM.?
The FDA product code for SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM. 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 Sea-Pac Trading Corp. 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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