PROTECTOR, SURGICAL INSTRUMENT
K-Number: K760320 · 1976-09-30
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Device Summary
Frequently Asked Questions
What is the PROTECTOR, SURGICAL INSTRUMENT?
PROTECTOR, SURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1976-09-30. The listed applicant is Devon Industries, Inc.. The 510(k) number is K760320.
When did PROTECTOR, SURGICAL INSTRUMENT receive FDA 510(k) clearance?
PROTECTOR, SURGICAL INSTRUMENT received FDA 510(k) clearance on 1976-09-30, under 510(k) number K760320.
Who is the listed applicant for PROTECTOR, SURGICAL INSTRUMENT?
The FDA 510(k) record lists Devon Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTECTOR, SURGICAL INSTRUMENT?
The FDA product code for PROTECTOR, SURGICAL INSTRUMENT is KCT.
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 Devon Industries, 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: KCT)
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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