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)

PROSTHOFLEX

K-Number: K942562 · 1994-12-20

ApplicantKnopf Assoc, Inc.
Decision Date1994-12-20
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROSTHOFLEX is the device name listed in this FDA 510(k) record. The listed applicant is Knopf Assoc, Inc.. It received FDA 510(k) clearance on 1994-12-20 under 510(k) number K942562. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSTHOFLEX?

PROSTHOFLEX is a medical device that received FDA 510(k) clearance on 1994-12-20. The listed applicant is Knopf Assoc, Inc.. The 510(k) number is K942562.

When did PROSTHOFLEX receive FDA 510(k) clearance?

PROSTHOFLEX received FDA 510(k) clearance on 1994-12-20, under 510(k) number K942562.

Who is the listed applicant for PROSTHOFLEX?

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

What is the FDA product code for PROSTHOFLEX?

The FDA product code for PROSTHOFLEX is EBI.

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: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, 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.

↑