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FDA 510(k)

CUSTOM PROCEDURE MEDICAL TRAY OR KIT

K-Number: K931844 · 1994-01-25

Decision Date1994-01-25
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

CUSTOM PROCEDURE MEDICAL TRAY OR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Custom Medical Products, Ltd.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K931844. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CUSTOM PROCEDURE MEDICAL TRAY OR KIT?

CUSTOM PROCEDURE MEDICAL TRAY OR KIT is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Custom Medical Products, Ltd.. The 510(k) number is K931844.

When did CUSTOM PROCEDURE MEDICAL TRAY OR KIT receive FDA 510(k) clearance?

CUSTOM PROCEDURE MEDICAL TRAY OR KIT received FDA 510(k) clearance on 1994-01-25, under 510(k) number K931844.

Who is the listed applicant for CUSTOM PROCEDURE MEDICAL TRAY OR KIT?

The FDA 510(k) record lists Custom Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSTOM PROCEDURE MEDICAL TRAY OR KIT?

The FDA product code for CUSTOM PROCEDURE MEDICAL TRAY OR KIT is LRO.

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 Custom Medical Products, Ltd. 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.

View all 13 devices →

Related Devices (Code: LRO)

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

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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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