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)

AUTONORM & NERV-A-NORM

K-Number: K811956 · 1981-07-31

ApplicantAutonomic Equipment Supply Co,
Decision Date1981-07-31
Product CodeKNM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AUTONORM & NERV-A-NORM is the device name listed in this FDA 510(k) record. The listed applicant is Autonomic Equipment Supply Co,. It received FDA 510(k) clearance on 1981-07-31 under 510(k) number K811956. The device is classified under product code KNM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTONORM & NERV-A-NORM?

AUTONORM & NERV-A-NORM is a medical device that received FDA 510(k) clearance on 1981-07-31. The listed applicant is Autonomic Equipment Supply Co,. The 510(k) number is K811956.

When did AUTONORM & NERV-A-NORM receive FDA 510(k) clearance?

AUTONORM & NERV-A-NORM received FDA 510(k) clearance on 1981-07-31, under 510(k) number K811956.

Who is the listed applicant for AUTONORM & NERV-A-NORM?

The FDA 510(k) record lists Autonomic Equipment Supply Co, as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTONORM & NERV-A-NORM?

The FDA product code for AUTONORM & NERV-A-NORM is KNM.

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 Autonomic Equipment Supply Co, 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.

K780312AUTONOM

Related Devices (Code: KNM)

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.

K780312AUTONOMAutonomic Equipment Supply Co,

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.

↑