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)

EMMETT IUD THREAD RETREIVER

K-Number: K820115 · 1982-02-05

ApplicantProto-Med, Inc.
Decision Date1982-02-05
Product CodeHHF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EMMETT IUD THREAD RETREIVER is the device name listed in this FDA 510(k) record. The listed applicant is Proto-Med, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820115. The device is classified under product code HHF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMMETT IUD THREAD RETREIVER?

EMMETT IUD THREAD RETREIVER is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Proto-Med, Inc.. The 510(k) number is K820115.

When did EMMETT IUD THREAD RETREIVER receive FDA 510(k) clearance?

EMMETT IUD THREAD RETREIVER received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820115.

Who is the listed applicant for EMMETT IUD THREAD RETREIVER?

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

What is the FDA product code for EMMETT IUD THREAD RETREIVER?

The FDA product code for EMMETT IUD THREAD RETREIVER is HHF.

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 Proto-Med, 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.

K844852THE GENERIC OXYGEN CONCENTRATORK822301ROYAL 1 OXYGEN CONCENTRATORK811761THE EMMETT IUD THREAD RETRIEVER

Related Devices (Code: HHF)

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.

K926541IUD HOOKSThomasville Medical Assoc.K891030IUD HOOKS - SIMPLE, UNIVERSAL AND SKLARZinnanti Surgical Instruments, Inc.K842295INTRAUTERINE DEVICE REMOVERPremier Dental Products Co.K831568RELIANCE TEMPO OPHTH. INSTR STANDF. & F. KoenigkramerK811761THE EMMETT IUD THREAD RETRIEVERProto-Med, 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.

↑