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FDA 510(k)

FOWLER ENDOCURETTE, MODEL CUR-XXX

K-Number: K000974 · 2000-05-23

ApplicantUtah Medical Products, Inc.
Decision Date2000-05-23
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FOWLER ENDOCURETTE, MODEL CUR-XXX is the device name listed in this FDA 510(k) record. The listed applicant is Utah Medical Products, Inc.. It received FDA 510(k) clearance on 2000-05-23 under 510(k) number K000974. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOWLER ENDOCURETTE, MODEL CUR-XXX?

FOWLER ENDOCURETTE, MODEL CUR-XXX is a medical device that received FDA 510(k) clearance on 2000-05-23. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K000974.

When did FOWLER ENDOCURETTE, MODEL CUR-XXX receive FDA 510(k) clearance?

FOWLER ENDOCURETTE, MODEL CUR-XXX received FDA 510(k) clearance on 2000-05-23, under 510(k) number K000974.

Who is the listed applicant for FOWLER ENDOCURETTE, MODEL CUR-XXX?

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

What is the FDA product code for FOWLER ENDOCURETTE, MODEL CUR-XXX?

The FDA product code for FOWLER ENDOCURETTE, MODEL CUR-XXX is HHK.

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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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