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FDA 510(k)

MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT

K-Number: K844597 · 1985-04-08

ApplicantXanmed Corp.
Decision Date1985-04-08
Product Code
DecisionSubstantially Equivalent

Device Summary

MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT is the device name listed in this FDA 510(k) record. The listed applicant is Xanmed Corp.. It received FDA 510(k) clearance on 1985-04-08 under 510(k) number K844597. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT?

MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT is a medical device that received FDA 510(k) clearance on 1985-04-08. The listed applicant is Xanmed Corp.. The 510(k) number is K844597.

When did MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT receive FDA 510(k) clearance?

MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT received FDA 510(k) clearance on 1985-04-08, under 510(k) number K844597.

Who is the listed applicant for MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT?

The FDA 510(k) record lists Xanmed Corp. as the applicant. This does not by itself establish the device manufacturer.

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 Xanmed 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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