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)

PORT-A-CATH IMPLANTABLE CATHETER SYS

K-Number: K832906 · 1984-03-06

ApplicantPharmacia, Inc.
Decision Date1984-03-06
Product CodeLLD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PORT-A-CATH IMPLANTABLE CATHETER SYS is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1984-03-06 under 510(k) number K832906. The device is classified under product code LLD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORT-A-CATH IMPLANTABLE CATHETER SYS?

PORT-A-CATH IMPLANTABLE CATHETER SYS is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is Pharmacia, Inc.. The 510(k) number is K832906.

When did PORT-A-CATH IMPLANTABLE CATHETER SYS receive FDA 510(k) clearance?

PORT-A-CATH IMPLANTABLE CATHETER SYS received FDA 510(k) clearance on 1984-03-06, under 510(k) number K832906.

Who is the listed applicant for PORT-A-CATH IMPLANTABLE CATHETER SYS?

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

What is the FDA product code for PORT-A-CATH IMPLANTABLE CATHETER SYS?

The FDA product code for PORT-A-CATH IMPLANTABLE CATHETER SYS is LLD.

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 Pharmacia, 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

View all 129 devices →

Related Devices (Code: LLD)

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.

K880072PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEMPharmacia Deltec, Inc.K864552PORT-A-CATH IMPLANTABLE CATHETER SYSTEMPharmacia, Inc.K862412INTESTOPLANTBurron Medical Products, 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.

↑