HANDLES, BLADE, SURGICAL
K-Number: K770800 · 1977-05-06
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Device Summary
Frequently Asked Questions
What is the HANDLES, BLADE, SURGICAL?
HANDLES, BLADE, SURGICAL is a medical device that received FDA 510(k) clearance on 1977-05-06. The listed applicant is Lukens Corp.. The 510(k) number is K770800.
When did HANDLES, BLADE, SURGICAL receive FDA 510(k) clearance?
HANDLES, BLADE, SURGICAL received FDA 510(k) clearance on 1977-05-06, under 510(k) number K770800.
Who is the listed applicant for HANDLES, BLADE, SURGICAL?
The FDA 510(k) record lists Lukens Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HANDLES, BLADE, SURGICAL?
The FDA product code for HANDLES, BLADE, SURGICAL 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 Lukens 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: 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.
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