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FDA 510(k)

EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT

K-Number: K844596 · 1985-08-01

ApplicantXanmed Corp.
Decision Date1985-08-01
Product Code
DecisionUnknown

Device Summary

EMERGENCY ROOM & MINOR OFFICE PROCEDURE 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 1985-08-01 under 510(k) number K844596. FDA Decision: Unknown.

Frequently Asked Questions

What is the EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT?

EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT is a medical device that received FDA 510(k) clearance on 1985-08-01. The listed applicant is Xanmed Corp.. The 510(k) number is K844596.

When did EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT receive FDA 510(k) clearance?

EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT received FDA 510(k) clearance on 1985-08-01, under 510(k) number K844596.

Who is the listed applicant for EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT?

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

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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.

K864623OBSTETRICAL/GYNECOLOGICAL CUSTOM SURGICAL KITK844595ORTHOPEDIC CUSTOM SURGICAL KITK844593CARDIOVASCULAR CUSTOM SURGICAL KITK844594NEURO CUSTOM SURGICAL KITK851906SURGICAL EYE PACKK844597MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT

View all 9 devices →

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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