FDA 510(k)

PRO MED 100

K-Number: K822854 · 1982-10-15

Decision Date1982-10-15

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

PRO MED 100 is the device name listed in this FDA 510(k) record. The listed applicant is Rebco Trading Co.. It received FDA 510(k) clearance on 1982-10-15 under 510(k) number K822854. 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 PRO MED 100?

PRO MED 100 is a medical device that received FDA 510(k) clearance on 1982-10-15. The listed applicant is Rebco Trading Co.. The 510(k) number is K822854.

When did PRO MED 100 receive FDA 510(k) clearance?

PRO MED 100 received FDA 510(k) clearance on 1982-10-15, under 510(k) number K822854.

Who is the listed applicant for PRO MED 100?

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

What is the FDA product code for PRO MED 100?

The FDA product code for PRO MED 100 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.