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)

PMT 3721-1 EPIDURAL KIT

K-Number: K883314 · 1988-10-28

ApplicantProgress Mankind Technology
Decision Date1988-10-28
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PMT 3721-1 EPIDURAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1988-10-28 under 510(k) number K883314. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT 3721-1 EPIDURAL KIT?

PMT 3721-1 EPIDURAL KIT is a medical device that received FDA 510(k) clearance on 1988-10-28. The listed applicant is Progress Mankind Technology. The 510(k) number is K883314.

When did PMT 3721-1 EPIDURAL KIT receive FDA 510(k) clearance?

PMT 3721-1 EPIDURAL KIT received FDA 510(k) clearance on 1988-10-28, under 510(k) number K883314.

Who is the listed applicant for PMT 3721-1 EPIDURAL KIT?

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

What is the FDA product code for PMT 3721-1 EPIDURAL KIT?

The FDA product code for PMT 3721-1 EPIDURAL KIT is CAZ.

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 Progress Mankind Technology 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.

K881616PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1K871663PMT TRACTION TONGSK854157PMT ACCUPRESSURE INFUSION SYSTEM 3601K845035ELECTRODE FOR NEUROLOGICAL SURGERY 2111K845036TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600K834047PMT-HALO/ORTHOPEDIC JACKET SYSTEM

View all 17 devices →

Related Devices (Code: CAZ)

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

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.

↑