FDA 510(k)

USG 2000SA

K-Number: K023227 · 2002-10-22

Decision Date2002-10-22

Product CodeHHJ

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

USG 2000SA is the device name listed in this FDA 510(k) record. The listed applicant is Ultraguide , Ltd.. It received FDA 510(k) clearance on 2002-10-22 under 510(k) number K023227. The device is classified under product code HHJ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USG 2000SA?

USG 2000SA is a medical device that received FDA 510(k) clearance on 2002-10-22. The listed applicant is Ultraguide , Ltd.. The 510(k) number is K023227.

When did USG 2000SA receive FDA 510(k) clearance?

USG 2000SA received FDA 510(k) clearance on 2002-10-22, under 510(k) number K023227.

Who is the listed applicant for USG 2000SA?

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

What is the FDA product code for USG 2000SA?

The FDA product code for USG 2000SA is HHJ.

Other records listing Ultraguide , Ltd. 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.

K022354ULTRAGUIDE CTG 2000SA K013150MR-GUIDE 2000 K011418ULTRAGUIDE MR-GUIDE 3000 K002258ULTRAGUIDE CT-GUIDE 1010 K974432ULTRAGUIDE 1000

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.