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FDA 510(k)

MICROTENS 7757 T.E.N.S. STIMULATOR

K-Number: K844017 · 1984-11-30

ApplicantRabar, Inc.
Decision Date1984-11-30
Product CodeGFJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROTENS 7757 T.E.N.S. STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Rabar, Inc.. It received FDA 510(k) clearance on 1984-11-30 under 510(k) number K844017. The device is classified under product code GFJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTENS 7757 T.E.N.S. STIMULATOR?

MICROTENS 7757 T.E.N.S. STIMULATOR is a medical device that received FDA 510(k) clearance on 1984-11-30. The listed applicant is Rabar, Inc.. The 510(k) number is K844017.

When did MICROTENS 7757 T.E.N.S. STIMULATOR receive FDA 510(k) clearance?

MICROTENS 7757 T.E.N.S. STIMULATOR received FDA 510(k) clearance on 1984-11-30, under 510(k) number K844017.

Who is the listed applicant for MICROTENS 7757 T.E.N.S. STIMULATOR?

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

What is the FDA product code for MICROTENS 7757 T.E.N.S. STIMULATOR?

The FDA product code for MICROTENS 7757 T.E.N.S. STIMULATOR is GFJ.

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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Other records listing Rabar, 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.

K842414ECHO PULSE BURSTK821736ECHO-PULSE KM555

Related Devices (Code: GFJ)

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.

K85178929-200 TO 29-230 VARIOUS BONE MALLETS(WIHIGER, DOYArtiberiaK822204ENT MALLETSKelleher Corp.

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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