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FDA 510(k)

Q-MS NEUROMUSCULAR STIMULATOR

K-Number: K912462 · 1992-06-04

Decision Date1992-06-04
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Q-MS NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Quantitative Medicine, Inc.. It received FDA 510(k) clearance on 1992-06-04 under 510(k) number K912462. 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 Q-MS NEUROMUSCULAR STIMULATOR?

Q-MS NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 1992-06-04. The listed applicant is Quantitative Medicine, Inc.. The 510(k) number is K912462.

When did Q-MS NEUROMUSCULAR STIMULATOR receive FDA 510(k) clearance?

Q-MS NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 1992-06-04, under 510(k) number K912462.

Who is the listed applicant for Q-MS NEUROMUSCULAR STIMULATOR?

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

What is the FDA product code for Q-MS NEUROMUSCULAR STIMULATOR?

The FDA product code for Q-MS NEUROMUSCULAR STIMULATOR is IPF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Quantitative Medicine, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: IPF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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