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FDA 510(k)

LIBERTY RECTAL PELVIC FLOOR EXERCISER

K-Number: K964526 · 1997-02-10

ApplicantUtah Medical Products, Inc.
Decision Date1997-02-10
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LIBERTY RECTAL PELVIC FLOOR EXERCISER 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 1997-02-10 under 510(k) number K964526. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERTY RECTAL PELVIC FLOOR EXERCISER?

LIBERTY RECTAL PELVIC FLOOR EXERCISER is a medical device that received FDA 510(k) clearance on 1997-02-10. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K964526.

When did LIBERTY RECTAL PELVIC FLOOR EXERCISER receive FDA 510(k) clearance?

LIBERTY RECTAL PELVIC FLOOR EXERCISER received FDA 510(k) clearance on 1997-02-10, under 510(k) number K964526.

Who is the listed applicant for LIBERTY RECTAL PELVIC FLOOR EXERCISER?

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 LIBERTY RECTAL PELVIC FLOOR EXERCISER?

The FDA product code for LIBERTY RECTAL PELVIC FLOOR EXERCISER is KPI.

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Other records listing Utah Medical Products, Inc. as applicant

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K123310FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+)K101535BT-CATHK063611SALINE/ CONTRAST MEDIA INFUSION CATHETERK001874PERIPHERALLY INSERTED CENTRAL CATHETERK000974FOWLER ENDOCURETTE, MODEL CUR-XXXK965245TBD

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Related Devices (Code: KPI)

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.

K262353BTL-299-FBTL Industries, Inc.K260178Pelvic Muscle Trainer (KM510, KM516B)Shenzhen Konmed Technology Co., Ltd.K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer (PC22E); Pelvic Muscle Trainer (PC22E-L)Hunan Accurate Bio-Medical Technology Co., Ltd.K252552Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)Shenzhen Changkun Technology Co., Ltd.K252831Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927)Dolanvy (Suzhou) Medical Technology Co., Ltd.K252334PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)Pontemedag

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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