FACELIFT SCISSORS
K-Number: K780152 · 1978-02-02
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Device Summary
Frequently Asked Questions
What is the FACELIFT SCISSORS?
FACELIFT SCISSORS is a medical device that received FDA 510(k) clearance on 1978-02-02. The listed applicant is Edward Weck, Inc.. The 510(k) number is K780152.
When did FACELIFT SCISSORS receive FDA 510(k) clearance?
FACELIFT SCISSORS received FDA 510(k) clearance on 1978-02-02, under 510(k) number K780152.
Who is the listed applicant for FACELIFT SCISSORS?
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 FACELIFT SCISSORS?
The FDA product code for FACELIFT SCISSORS 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.
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