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FDA 510(k)

DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM

K-Number: K912342 · 1991-12-09

ApplicantAmer Inst of Electrodiagnosis/Electrotherapy, Inc.
Decision Date1991-12-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM is the device name listed in this FDA 510(k) record. The listed applicant is Amer Inst of Electrodiagnosis/Electrotherapy, Inc.. It received FDA 510(k) clearance on 1991-12-09 under 510(k) number K912342. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM?

DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM is a medical device that received FDA 510(k) clearance on 1991-12-09. The listed applicant is Amer Inst of Electrodiagnosis/Electrotherapy, Inc.. The 510(k) number is K912342.

When did DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM receive FDA 510(k) clearance?

DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM received FDA 510(k) clearance on 1991-12-09, under 510(k) number K912342.

Who is the listed applicant for DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM?

The FDA 510(k) record lists Amer Inst of Electrodiagnosis/Electrotherapy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM?

The FDA product code for DR. LIBERSON'S MICROPULSE NEUROMUSCULAR TRANS STIM is IPF.

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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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