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)

MENTOR ACTIVATOR NEUROMUSCULAR STIMU

K-Number: K820168 · 1982-02-24

ApplicantMentor Corp.
Decision Date1982-02-24
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MENTOR ACTIVATOR NEUROMUSCULAR STIMU is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 1982-02-24 under 510(k) number K820168. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR ACTIVATOR NEUROMUSCULAR STIMU?

MENTOR ACTIVATOR NEUROMUSCULAR STIMU is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Mentor Corp.. The 510(k) number is K820168.

When did MENTOR ACTIVATOR NEUROMUSCULAR STIMU receive FDA 510(k) clearance?

MENTOR ACTIVATOR NEUROMUSCULAR STIMU received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820168.

Who is the listed applicant for MENTOR ACTIVATOR NEUROMUSCULAR STIMU?

The FDA 510(k) record lists Mentor Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENTOR ACTIVATOR NEUROMUSCULAR STIMU?

The FDA product code for MENTOR ACTIVATOR NEUROMUSCULAR STIMU 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 Mentor Corp. 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.

View all 61 devices →

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.

↑