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FDA 510(k)

KSEA MODEL 383320 20 ANGIOMAT

K-Number: K960486 · 1996-10-25

ApplicantKarl Storz Endoscopy
Decision Date1996-10-25
Product CodeDQI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KSEA MODEL 383320 20 ANGIOMAT is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 1996-10-25 under 510(k) number K960486. The device is classified under product code DQI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KSEA MODEL 383320 20 ANGIOMAT?

KSEA MODEL 383320 20 ANGIOMAT is a medical device that received FDA 510(k) clearance on 1996-10-25. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K960486.

When did KSEA MODEL 383320 20 ANGIOMAT receive FDA 510(k) clearance?

KSEA MODEL 383320 20 ANGIOMAT received FDA 510(k) clearance on 1996-10-25, under 510(k) number K960486.

Who is the listed applicant for KSEA MODEL 383320 20 ANGIOMAT?

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

What is the FDA product code for KSEA MODEL 383320 20 ANGIOMAT?

The FDA product code for KSEA MODEL 383320 20 ANGIOMAT is DQI.

Related Clinical Trials

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Other records listing Karl Storz Endoscopy 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.

K043375FISCH TITANIUM MIDDLE EAR PROSTHESESK030848PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIXK030009KSEA POWERSHAVER SYSTEM S2K023924AUTOCON II 200 ELECTROSURGICAL GENERATORK023187KSEA SPINOSCOPEK011700MODULITH SLK LITHOTRIPTER

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Related Devices (Code: DQI)

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.

K935763SURGIPUMPW.O.M. World of Medicine GmbHK922541USCI SUPER 9 PTCA GUIDING CATHETERC.R. Bard, Inc.K924110LEOCOR CORFLO PUMP -- MODIFICATIONLeocor, Inc.K905189BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)Baxter Healthcare CorpK902444CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMPIntramed Laboratories, Inc.K895688NOBLES-LAI ENGINEERING INFUSION PUMPNobles-Lai Engineering, 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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