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FDA 510(k)

WATSYSTEM

K-Number: K926136 · 1994-05-20

ApplicantWatsystem Div. of Itc
Decision Date1994-05-20
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WATSYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Watsystem Div. of Itc. It received FDA 510(k) clearance on 1994-05-20 under 510(k) number K926136. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATSYSTEM?

WATSYSTEM is a medical device that received FDA 510(k) clearance on 1994-05-20. The listed applicant is Watsystem Div. of Itc. The 510(k) number is K926136.

When did WATSYSTEM receive FDA 510(k) clearance?

WATSYSTEM received FDA 510(k) clearance on 1994-05-20, under 510(k) number K926136.

Who is the listed applicant for WATSYSTEM?

The FDA 510(k) record lists Watsystem Div. of Itc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WATSYSTEM?

The FDA product code for WATSYSTEM is BXB.

Related Clinical Trials

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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