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FDA 510(k)

LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR

K-Number: K910616 · 1992-05-12

ApplicantLife Balance Intl., Inc.
Decision Date1992-05-12
Product CodeQJQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Balance Intl., Inc.. It received FDA 510(k) clearance on 1992-05-12 under 510(k) number K910616. The device is classified under product code QJQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR?

LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR is a medical device that received FDA 510(k) clearance on 1992-05-12. The listed applicant is Life Balance Intl., Inc.. The 510(k) number is K910616.

When did LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR receive FDA 510(k) clearance?

LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR received FDA 510(k) clearance on 1992-05-12, under 510(k) number K910616.

Who is the listed applicant for LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR?

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

What is the FDA product code for LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR?

The FDA product code for LB-2000 CRANIAL ELECTROTHERAPY STIMULATOR is QJQ.

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Related Devices (Code: QJQ)

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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.

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