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FDA 510(k)

THE KARL STORZ HAMOU ENDOMAT

K-Number: K936231 · 1995-01-24

ApplicantKarl Storz Endoscopy
Decision Date1995-01-24
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE KARL STORZ HAMOU ENDOMAT 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 1995-01-24 under 510(k) number K936231. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE KARL STORZ HAMOU ENDOMAT?

THE KARL STORZ HAMOU ENDOMAT is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K936231.

When did THE KARL STORZ HAMOU ENDOMAT receive FDA 510(k) clearance?

THE KARL STORZ HAMOU ENDOMAT received FDA 510(k) clearance on 1995-01-24, under 510(k) number K936231.

Who is the listed applicant for THE KARL STORZ HAMOU ENDOMAT?

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 THE KARL STORZ HAMOU ENDOMAT?

The FDA product code for THE KARL STORZ HAMOU ENDOMAT is HIG.

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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: HIG)

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.

K261706Endomat Select (UP220)KARL STORZ SE & CO. KGK251273Asurys Fluid Management SystemBoston Scientific CorporationK240886Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)Hologic, Inc.K210628X-FLO Fluid Management SystemThermedx, LLCK201355Endomat Select, IBS Shaver Software, LicenseKarl Storz SE & CO. KGK180735Endomat SelectKarl Storz SE & CO. KG

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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