KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA
K-Number: K850049 · 1985-03-06
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Device Summary
Frequently Asked Questions
What is the KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA?
KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA is a medical device that received FDA 510(k) clearance on 1985-03-06. The listed applicant is Xtal Corp.. The 510(k) number is K850049.
When did KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA receive FDA 510(k) clearance?
KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA received FDA 510(k) clearance on 1985-03-06, under 510(k) number K850049.
Who is the listed applicant for KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA?
The FDA 510(k) record lists Xtal Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA?
The FDA product code for KATENA MICROMETER KNIFE W/XTAL BLADE OF CRYSTAL SA is HNN.
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 Xtal 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: HNN)
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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