Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

STIMULATOR, NERVE, TRANSCUTANEOUS

K-Number: K781157 · 1978-09-20

ApplicantMedtech Intl., Inc.
Decision Date1978-09-20
Product Code
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, NERVE, TRANSCUTANEOUS is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Intl., Inc.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781157. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULATOR, NERVE, TRANSCUTANEOUS?

STIMULATOR, NERVE, TRANSCUTANEOUS is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Medtech Intl., Inc.. The 510(k) number is K781157.

When did STIMULATOR, NERVE, TRANSCUTANEOUS receive FDA 510(k) clearance?

STIMULATOR, NERVE, TRANSCUTANEOUS received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781157.

Who is the listed applicant for STIMULATOR, NERVE, TRANSCUTANEOUS?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medtech Intl., 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.

K920876CUT RESISTANT GLOVES OR SURGICAL GLOVE LINERK853843IV MATEK791462HYPERDERMIC NEEDLE WITH SENSOR #514K790467SURGICAL EYE SPONGEK790389GAUZE & COTTON SPONGES

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.

↑