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FDA 510(k)

MEDICAL PROCEDURE TRAY, MODIFICATION

K-Number: K930884 · 1995-03-21

ApplicantEnpak Medical Corp.
Decision Date1995-03-21
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDICAL PROCEDURE TRAY, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Enpak Medical Corp.. It received FDA 510(k) clearance on 1995-03-21 under 510(k) number K930884. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL PROCEDURE TRAY, MODIFICATION?

MEDICAL PROCEDURE TRAY, MODIFICATION is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Enpak Medical Corp.. The 510(k) number is K930884.

When did MEDICAL PROCEDURE TRAY, MODIFICATION receive FDA 510(k) clearance?

MEDICAL PROCEDURE TRAY, MODIFICATION received FDA 510(k) clearance on 1995-03-21, under 510(k) number K930884.

Who is the listed applicant for MEDICAL PROCEDURE TRAY, MODIFICATION?

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

What is the FDA product code for MEDICAL PROCEDURE TRAY, MODIFICATION?

The FDA product code for MEDICAL PROCEDURE TRAY, MODIFICATION is LDQ.

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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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