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FDA 510(k)

SWIMEX MULTIDEPTH POOL (MODEL 600T)

K-Number: K935011 · 1995-01-09

ApplicantSwimex Systems
Decision Date1995-01-09
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SWIMEX MULTIDEPTH POOL (MODEL 600T) is the device name listed in this FDA 510(k) record. The listed applicant is Swimex Systems. It received FDA 510(k) clearance on 1995-01-09 under 510(k) number K935011. 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 SWIMEX MULTIDEPTH POOL (MODEL 600T)?

SWIMEX MULTIDEPTH POOL (MODEL 600T) is a medical device that received FDA 510(k) clearance on 1995-01-09. The listed applicant is Swimex Systems. The 510(k) number is K935011.

When did SWIMEX MULTIDEPTH POOL (MODEL 600T) receive FDA 510(k) clearance?

SWIMEX MULTIDEPTH POOL (MODEL 600T) received FDA 510(k) clearance on 1995-01-09, under 510(k) number K935011.

Who is the listed applicant for SWIMEX MULTIDEPTH POOL (MODEL 600T)?

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

What is the FDA product code for SWIMEX MULTIDEPTH POOL (MODEL 600T)?

The FDA product code for SWIMEX MULTIDEPTH POOL (MODEL 600T) is BXB.

Related Clinical Trials

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.

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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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