Q-MS NEUROMUSCULAR STIMULATOR
K-Number: K912462 · 1992-06-04
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Device Summary
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.
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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