NEUROGAR III-TRANSCUT. ELEC. NERVE STIM
K-Number: K801576 · 1980-08-14
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Device Summary
Frequently Asked Questions
What is the NEUROGAR III-TRANSCUT. ELEC. NERVE STIM?
NEUROGAR III-TRANSCUT. ELEC. NERVE STIM is a medical device that received FDA 510(k) clearance on 1980-08-14. The listed applicant is Inter Med Industries, Inc.. The 510(k) number is K801576.
When did NEUROGAR III-TRANSCUT. ELEC. NERVE STIM receive FDA 510(k) clearance?
NEUROGAR III-TRANSCUT. ELEC. NERVE STIM received FDA 510(k) clearance on 1980-08-14, under 510(k) number K801576.
Who is the listed applicant for NEUROGAR III-TRANSCUT. ELEC. NERVE STIM?
The FDA 510(k) record lists Inter Med Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUROGAR III-TRANSCUT. ELEC. NERVE STIM?
The FDA product code for NEUROGAR III-TRANSCUT. ELEC. NERVE STIM 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 Inter Med Industries, 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: 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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