PERSONNA DISPOSABLE SCALPEL
K-Number: K873142 · 1987-09-04
Advertisement
Device Summary
Frequently Asked Questions
What is the PERSONNA DISPOSABLE SCALPEL?
PERSONNA DISPOSABLE SCALPEL is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is American Safety Razor Co.. The 510(k) number is K873142.
When did PERSONNA DISPOSABLE SCALPEL receive FDA 510(k) clearance?
PERSONNA DISPOSABLE SCALPEL received FDA 510(k) clearance on 1987-09-04, under 510(k) number K873142.
Who is the listed applicant for PERSONNA DISPOSABLE SCALPEL?
The FDA 510(k) record lists American Safety Razor Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERSONNA DISPOSABLE SCALPEL?
The FDA product code for PERSONNA DISPOSABLE SCALPEL is GES.
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 American Safety Razor Co. 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: GES)
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