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FDA 510(k)

TRANSCUTANEOUS ELECT. NERVE STIMULATOR

K-Number: K803247 · 1981-03-20

ApplicantMedical Research Laboratories, Inc.
Decision Date1981-03-20
Product Code
DecisionSubstantially Equivalent

Device Summary

TRANSCUTANEOUS ELECT. NERVE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Research Laboratories, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K803247. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSCUTANEOUS ELECT. NERVE STIMULATOR?

TRANSCUTANEOUS ELECT. NERVE STIMULATOR is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Medical Research Laboratories, Inc.. The 510(k) number is K803247.

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

TRANSCUTANEOUS ELECT. NERVE STIMULATOR received FDA 510(k) clearance on 1981-03-20, under 510(k) number K803247.

Who is the listed applicant for TRANSCUTANEOUS ELECT. NERVE STIMULATOR?

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

Related Clinical Trials

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Other records listing Medical Research Laboratories, 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.

K021168JUMP START, MODEL 970300K012766PORTABLE INTENSIVE CARE UNITK012030PORTABLE INTENSIVE CARE UNITK010207PORTABLE INSTENSIVE CARE UNITK002232AEDEFIBRILLATORK000712PORTABLE INTENSIVE CARE UNIT, MODEL PIC

View all 19 devices →

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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