FDA 510(k)

ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103

K-Number: K992764 · 1999-10-14

Decision Date1999-10-14

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103 is the device name listed in this FDA 510(k) record. The listed applicant is Erbe USA, Inc.. It received FDA 510(k) clearance on 1999-10-14 under 510(k) number K992764. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103?

ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103 is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Erbe USA, Inc.. The 510(k) number is K992764.

When did ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103 receive FDA 510(k) clearance?

ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103 received FDA 510(k) clearance on 1999-10-14, under 510(k) number K992764.

Who is the listed applicant for ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103?

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

What is the FDA product code for ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103?

The FDA product code for ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103 is GEI.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Erbe USA, Inc. as applicant

K221177Erbe's Tubing/Cap Sets K191438ERBEFLO 2 Endo Quick Connect Pentax Scope Port Connector K190469ERBEFLO 2 Disposable Tubing System K182444ERBEFLO Olympus Scope Port Connector K162152Erbe’s CO2 Tubing/Cap Sets K132340ERBEFLO CLEVERCAP HYBRID TUBING/CAP SET FOR PENTAX SCOPES, ERBEFLO CLEVERCAP HYBRID CO2 TUBING/CAP SET FOR OLYMPUS 160/1

View all 36 devices →

Related Devices (Code: GEI)

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker Instruments K254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLC K261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLC K254185Potenza PrimeJeisys Medical Incorporated K262364Ellian Enigma RF DeviceEllian Corp K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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.