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)

DADC '500' DRIVING CONTROL

K-Number: K884899 · 1989-02-10

ApplicantDriving Aids Development Corp.
Decision Date1989-02-10
Product CodeIPQ
DecisionSubstantially Equivalent

Device Summary

DADC '500' DRIVING CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Driving Aids Development Corp.. It received FDA 510(k) clearance on 1989-02-10 under 510(k) number K884899. The device is classified under product code IPQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DADC '500' DRIVING CONTROL?

DADC '500' DRIVING CONTROL is a medical device that received FDA 510(k) clearance on 1989-02-10. The listed applicant is Driving Aids Development Corp.. The 510(k) number is K884899.

When did DADC '500' DRIVING CONTROL receive FDA 510(k) clearance?

DADC '500' DRIVING CONTROL received FDA 510(k) clearance on 1989-02-10, under 510(k) number K884899.

Who is the listed applicant for DADC '500' DRIVING CONTROL?

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

What is the FDA product code for DADC '500' DRIVING CONTROL?

The FDA product code for DADC '500' DRIVING CONTROL is IPQ.

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

Related Devices (Code: IPQ)

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.

K904934AUTOMASTERTeam Mfg., Inc.K910072SURE GRIP, HAND CONTROLS MODEL SG-1Howell Ventures , Ltd.K900416HAND CONTROLS, MODEL 3700 AND 3500 SERIESMobility Products & Design

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.

↑