STIMTECH NEUROMUSCULAR STIMULATOR, C 600
K-Number: K791048 · 1979-07-03
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Device Summary
Frequently Asked Questions
What is the STIMTECH NEUROMUSCULAR STIMULATOR, C 600?
STIMTECH NEUROMUSCULAR STIMULATOR, C 600 is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Stimulation Technology, Inc.. The 510(k) number is K791048.
When did STIMTECH NEUROMUSCULAR STIMULATOR, C 600 receive FDA 510(k) clearance?
STIMTECH NEUROMUSCULAR STIMULATOR, C 600 received FDA 510(k) clearance on 1979-07-03, under 510(k) number K791048.
Who is the listed applicant for STIMTECH NEUROMUSCULAR STIMULATOR, C 600?
The FDA 510(k) record lists Stimulation Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STIMTECH NEUROMUSCULAR STIMULATOR, C 600?
The FDA product code for STIMTECH NEUROMUSCULAR STIMULATOR, C 600 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 Stimulation Technology, 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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