HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3
K-Number: K003231 · 2001-01-12
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Device Summary
Frequently Asked Questions
What is the HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3?
HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3 is a medical device that received FDA 510(k) clearance on 2001-01-12. The listed applicant is Home Medical Services. The 510(k) number is K003231.
When did HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3 receive FDA 510(k) clearance?
HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3 received FDA 510(k) clearance on 2001-01-12, under 510(k) number K003231.
Who is the listed applicant for HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3?
The FDA 510(k) record lists Home Medical Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3?
The FDA product code for HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3 is GZJ.
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 Home Medical Services 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: GZJ)
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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