Who is the manufacturer of TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS?

Elscint, Inc. filed the 510(k) submission for TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS (K837180).

What is the regulatory pathway for TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS

K837180 · Elscint, Inc. · Mar 17, 1983 · RA

Device Facts

Record ID	K837180
Device Name	TREPHIX THREE PHSE GENERATORS AND EXONON SINGLE PHASE GENERATORS
Applicant	Elscint, Inc.
Decision Date	Mar 17, 1983
Decision	SESE
Submission Type	Traditional

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