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FDA 510(k)

URESIL ENDOSCOPIC LASER OVERTUBE

K-Number: K901882 · 1990-07-27

ApplicantUresil Corp.
Decision Date1990-07-27
Product CodeKOQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

URESIL ENDOSCOPIC LASER OVERTUBE is the device name listed in this FDA 510(k) record. The listed applicant is Uresil Corp.. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K901882. 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 URESIL ENDOSCOPIC LASER OVERTUBE?

URESIL ENDOSCOPIC LASER OVERTUBE is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Uresil Corp.. The 510(k) number is K901882.

When did URESIL ENDOSCOPIC LASER OVERTUBE receive FDA 510(k) clearance?

URESIL ENDOSCOPIC LASER OVERTUBE received FDA 510(k) clearance on 1990-07-27, under 510(k) number K901882.

Who is the listed applicant for URESIL ENDOSCOPIC LASER OVERTUBE?

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

What is the FDA product code for URESIL ENDOSCOPIC LASER OVERTUBE?

The FDA product code for URESIL ENDOSCOPIC LASER OVERTUBE is KOQ.

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Other records listing Uresil Corp. 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.

K003753GP GENERAL PURPOSE DRAINAGE SET, MINI-PIGTAIL DRAINAGE CATHETER WITH LOCKING PIGTAIL, GP GENERAL PURPOSE DRAINAGE CATHEK980278URESIL VASCU-FLO INFUSION CATHETERK981344URESIL PERCUTANEOUS DRAINAGE CATHETERS WITH HYDROPHILIC COATINGK980282URESIL DILATOR WITH RADIOPAQUE MARKERK980889URESIL NEPHRO-URETERAL STENTK972582URESIL GUIDEWIRE

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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.

K896821OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDENorth American Sterilization & Packaging Co.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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