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FDA 510(k)

ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.

K-Number: K873357 · 1987-10-26

ApplicantTh Charters, Inc.
Decision Date1987-10-26
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA. is the device name listed in this FDA 510(k) record. The listed applicant is Th Charters, Inc.. It received FDA 510(k) clearance on 1987-10-26 under 510(k) number K873357. 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 ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.?

ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA. is a medical device that received FDA 510(k) clearance on 1987-10-26. The listed applicant is Th Charters, Inc.. The 510(k) number is K873357.

When did ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA. receive FDA 510(k) clearance?

ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA. received FDA 510(k) clearance on 1987-10-26, under 510(k) number K873357.

Who is the listed applicant for ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.?

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

What is the FDA product code for ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.?

The FDA product code for ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA. is GZJ.

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Other records listing Th Charters, Inc. as applicant

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.

K861501EXER-STIM 2K851946REMOTE SPEED CONTROLK851967TORQUE FEEDBACK METERK834215MINI-1 TRANSCUTANEOUS ELEC-NERVE STIMK831850NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVEK822056EXER-STIM CONTROLLER

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Related Devices (Code: GZJ)

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K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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