FDA 510(k)

MEDA 2500 T.E.N.S.

K-Number: K862450 · 1986-11-25

Decision Date1986-11-25

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDA 2500 T.E.N.S. is the device name listed in this FDA 510(k) record. The listed applicant is Watlow/Winona, Inc.. It received FDA 510(k) clearance on 1986-11-25 under 510(k) number K862450. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDA 2500 T.E.N.S.?

MEDA 2500 T.E.N.S. is a medical device that received FDA 510(k) clearance on 1986-11-25. The listed applicant is Watlow/Winona, Inc.. The 510(k) number is K862450.

When did MEDA 2500 T.E.N.S. receive FDA 510(k) clearance?

MEDA 2500 T.E.N.S. received FDA 510(k) clearance on 1986-11-25, under 510(k) number K862450.

Who is the listed applicant for MEDA 2500 T.E.N.S.?

The FDA 510(k) record lists Watlow/Winona, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDA 2500 T.E.N.S.?

The FDA product code for MEDA 2500 T.E.N.S. is GZJ.

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimed K252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLC K232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical Officer K233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.