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)

FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.

K-Number: K760795 · 1976-10-20

ApplicantMidwest
Decision Date1976-10-20
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C. is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760795. The device is classified under product code EAY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.?

FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C. is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Midwest. The 510(k) number is K760795.

When did FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C. receive FDA 510(k) clearance?

FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C. received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760795.

Who is the listed applicant for FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.?

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

What is the FDA product code for FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.?

The FDA product code for FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C. is EAY.

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 Midwest 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.

K863677TRADITION HIGH SPEED HANDPIECEK850344AM-40 POWER OPTIC AIR MOTOR POWER OPTIC CONTRA ANGK792445MW STRAIGHT ATTACHMENTK792303MW 8000-IK792302LS-100K792304MW-8000

View all 13 devices →

Related Devices (Code: EAY)

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.

K953192MODEL A15-103Beaverstate Dental, Inc.K953191MODEL A15-101Beaverstate Dental, Inc.K935718JEDENTAL VLC DENTAL CURING LIGHTJedental Co., Inc.K871816STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TMStryker Corp.K831976POWER OPTICRitter Co.K831824DENTAL ELECTRONIC/S.B.R TRADING BU HANDSilverman'S

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.

↑