FDA 510(k)

STERILE INSTRUMENT DRAPE

K-Number: K902763 · 1990-09-20

ApplicantNorth American Sterilization & Packaging Co.

Decision Date1990-09-20

Product CodeHMW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STERILE INSTRUMENT DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is North American Sterilization & Packaging Co.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K902763. The device is classified under product code HMW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE INSTRUMENT DRAPE?

STERILE INSTRUMENT DRAPE is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is North American Sterilization & Packaging Co.. The 510(k) number is K902763.

When did STERILE INSTRUMENT DRAPE receive FDA 510(k) clearance?

STERILE INSTRUMENT DRAPE received FDA 510(k) clearance on 1990-09-20, under 510(k) number K902763.

Who is the listed applicant for STERILE INSTRUMENT DRAPE?

The FDA 510(k) record lists North American Sterilization & Packaging Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE INSTRUMENT DRAPE?

The FDA product code for STERILE INSTRUMENT DRAPE is HMW.

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Other records listing North American Sterilization & Packaging Co. as applicant

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Related Devices (Code: HMW)

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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.