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FDA 510(k)

MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR

K-Number: K920436 · 1992-05-20

ApplicantMedtronic Vascular
Decision Date1992-05-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1992-05-20 under 510(k) number K920436. 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 MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR?

MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 1992-05-20. The listed applicant is Medtronic Vascular. The 510(k) number is K920436.

When did MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR receive FDA 510(k) clearance?

MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 1992-05-20, under 510(k) number K920436.

Who is the listed applicant for MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR?

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

What is the FDA product code for MEDTRONIC RESPOND III NEUROMUSCULAR STIMULATOR?

The FDA product code for MEDTRONIC RESPOND III 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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