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FDA 510(k)

OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE

K-Number: K896821 · 1990-02-09

ApplicantNorth American Sterilization & Packaging Co.
Decision Date1990-02-09
Product CodeKOQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE 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 1990-02-09 under 510(k) number K896821. The device is classified under product code KOQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE?

OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is North American Sterilization & Packaging Co.. The 510(k) number is K896821.

When did OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE receive FDA 510(k) clearance?

OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE received FDA 510(k) clearance on 1990-02-09, under 510(k) number K896821.

Who is the listed applicant for OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE?

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 OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE?

The FDA product code for OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDE is KOQ.

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Other records listing North American Sterilization & Packaging Co. 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.

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Related Devices (Code: KOQ)

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.

K901882URESIL ENDOSCOPIC LASER OVERTUBEUresil Corp.K900401NAS&P GRASPING FORCEPS & ASSOC. DEVICESNorth American Sterilization & Packaging Co.K831265DENTOLOCK DENTURE ADHESIVE CREAMSolar Dental Co., Inc.

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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