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FDA 510(k)

VARIOUS NON-STERILE CUSTOM TRAYS/KITS

K-Number: K924690 · 1993-07-16

Decision Date1993-07-16
Product CodeMCY
Advisory CommitteeHO
DecisionUnknown

Device Summary

VARIOUS NON-STERILE CUSTOM TRAYS/KITS is the device name listed in this FDA 510(k) record. The listed applicant is Surgipro Central, Inc.. It received FDA 510(k) clearance on 1993-07-16 under 510(k) number K924690. The device is classified under product code MCY. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VARIOUS NON-STERILE CUSTOM TRAYS/KITS?

VARIOUS NON-STERILE CUSTOM TRAYS/KITS is a medical device that received FDA 510(k) clearance on 1993-07-16. The listed applicant is Surgipro Central, Inc.. The 510(k) number is K924690.

When did VARIOUS NON-STERILE CUSTOM TRAYS/KITS receive FDA 510(k) clearance?

VARIOUS NON-STERILE CUSTOM TRAYS/KITS received FDA 510(k) clearance on 1993-07-16, under 510(k) number K924690.

Who is the listed applicant for VARIOUS NON-STERILE CUSTOM TRAYS/KITS?

The FDA 510(k) record lists Surgipro Central, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VARIOUS NON-STERILE CUSTOM TRAYS/KITS?

The FDA product code for VARIOUS NON-STERILE CUSTOM TRAYS/KITS is MCY.

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.

Related Devices (Code: MCY)

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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