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)

VYGON THORACIC DRAINAGE-VARIOUS #'S

K-Number: K832628 · 1984-01-30

ApplicantExco, Inc.
Decision Date1984-01-30
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VYGON THORACIC DRAINAGE-VARIOUS #'S is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K832628. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON THORACIC DRAINAGE-VARIOUS #'S?

VYGON THORACIC DRAINAGE-VARIOUS #'S is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Exco, Inc.. The 510(k) number is K832628.

When did VYGON THORACIC DRAINAGE-VARIOUS #'S receive FDA 510(k) clearance?

VYGON THORACIC DRAINAGE-VARIOUS #'S received FDA 510(k) clearance on 1984-01-30, under 510(k) number K832628.

Who is the listed applicant for VYGON THORACIC DRAINAGE-VARIOUS #'S?

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

What is the FDA product code for VYGON THORACIC DRAINAGE-VARIOUS #'S?

The FDA product code for VYGON THORACIC DRAINAGE-VARIOUS #'S is KDD.

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 Exco, 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.

K844203ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403K844175ENTERNAL FEEDING TUBE-POLYURETHANE EF504K844174FLEXIBLE STAINLESS STEEL STYLET FOR ENTERNAL FEEDIK831802LIFE VAC #2191 & 2192K833079CENTRACATH #130,135 & 137-HEMOCATH #K830910MANOMETER SET C.V.P. #S 298/299

View all 20 devices →

Related Devices (Code: KDD)

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.

K072814CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURESCovidienK011514INSTRUMENTS FOR ONE TIME USE - DISPOSABLEKencap , Ltd.K971317NATIONAL MEDICAL HEALTHCARE CUSTOM ORTHOPEDIC KITS AND TRAYSNational Healthcare Mfg. Corp.K960456DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAYDenver Biomaterials, Inc.K936255CUSTOM CV PACKAssociated MedicalK932219SUTURE SET OR LACERATION TRAYS (PACKS)Associated Medical Products Co.

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.

↑