HARMONIC SCALPEL BLADES AND SHEARS
K-Number: K060245 · 2006-04-07
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Device Summary
Frequently Asked Questions
What is the HARMONIC SCALPEL BLADES AND SHEARS?
HARMONIC SCALPEL BLADES AND SHEARS is a medical device that received FDA 510(k) clearance on 2006-04-07. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K060245.
When did HARMONIC SCALPEL BLADES AND SHEARS receive FDA 510(k) clearance?
HARMONIC SCALPEL BLADES AND SHEARS received FDA 510(k) clearance on 2006-04-07, under 510(k) number K060245.
Who is the listed applicant for HARMONIC SCALPEL BLADES AND SHEARS?
The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HARMONIC SCALPEL BLADES AND SHEARS?
The FDA product code for HARMONIC SCALPEL BLADES AND SHEARS is LFL.
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 Ethicon Endo-Surgery, 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: LFL)
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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