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)

DISPOSABLE FLOOR INSTRUMENTS

K-Number: K831911 · 1983-09-12

ApplicantOrmed Mfg., Inc.
Decision Date1983-09-12
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE FLOOR INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Ormed Mfg., Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831911. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE FLOOR INSTRUMENTS?

DISPOSABLE FLOOR INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Ormed Mfg., Inc.. The 510(k) number is K831911.

When did DISPOSABLE FLOOR INSTRUMENTS receive FDA 510(k) clearance?

DISPOSABLE FLOOR INSTRUMENTS received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831911.

Who is the listed applicant for DISPOSABLE FLOOR INSTRUMENTS?

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

What is the FDA product code for DISPOSABLE FLOOR INSTRUMENTS?

The FDA product code for DISPOSABLE FLOOR INSTRUMENTS is KDC.

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 Ormed Mfg., 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.

K931555ARTROMOT K2 CPMK882529BUTCHER STRUNG TONSIL SPONGEK882527GAUZE SPONGEK882528CYLINDRICAL SPONGEK882530TAPE STRUNG TONSIL SPONGEK880853CHERRY SPONGE

View all 23 devices →

Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.

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.

↑