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FDA 510(k)

XH-1 NEUROMUSCULAR STIMULATOR

K-Number: K950550 · 1996-12-04

ApplicantCalifornia Medical Research Institute
Decision Date1996-12-04
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

XH-1 NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is California Medical Research Institute. It received FDA 510(k) clearance on 1996-12-04 under 510(k) number K950550. 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 XH-1 NEUROMUSCULAR STIMULATOR?

XH-1 NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 1996-12-04. The listed applicant is California Medical Research Institute. The 510(k) number is K950550.

When did XH-1 NEUROMUSCULAR STIMULATOR receive FDA 510(k) clearance?

XH-1 NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 1996-12-04, under 510(k) number K950550.

Who is the listed applicant for XH-1 NEUROMUSCULAR STIMULATOR?

The FDA 510(k) record lists California Medical Research Institute as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XH-1 NEUROMUSCULAR STIMULATOR?

The FDA product code for XH-1 NEUROMUSCULAR STIMULATOR 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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