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)

MANOMETER SET C.V.P. #S 298/299

K-Number: K830910 · 1983-04-05

ApplicantExco, Inc.
Decision Date1983-04-05
Product CodeKRK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MANOMETER SET C.V.P. #S 298/299 is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K830910. The device is classified under product code KRK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANOMETER SET C.V.P. #S 298/299?

MANOMETER SET C.V.P. #S 298/299 is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Exco, Inc.. The 510(k) number is K830910.

When did MANOMETER SET C.V.P. #S 298/299 receive FDA 510(k) clearance?

MANOMETER SET C.V.P. #S 298/299 received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830910.

Who is the listed applicant for MANOMETER SET C.V.P. #S 298/299?

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 MANOMETER SET C.V.P. #S 298/299?

The FDA product code for MANOMETER SET C.V.P. #S 298/299 is KRK.

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.

K844175ENTERNAL FEEDING TUBE-POLYURETHANE EF504K844203ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403K844174FLEXIBLE STAINLESS STEEL STYLET FOR ENTERNAL FEEDIK832628VYGON THORACIC DRAINAGE-VARIOUS #'SK831802LIFE VAC #2191 & 2192K833079CENTRACATH #130,135 & 137-HEMOCATH #

View all 20 devices →

Related Devices (Code: KRK)

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.

K950607UST-5268P-5 TRANSDUCERAloka Co., Ltd.K904674CENTRAL VENOUS PRESSURE MANOMETERMedex, Inc.K884386ADMINISTRATION/MANOMETER SET W/3 WAY STOPCOCKEthitek Pharmaceuticals Co.K875322MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETERSchneider-Shilley (Usa)K861605SCHNEIDER-SHILEY PRESSURE MANOMETERShiley, Inc.K813498MEDIFIXBurron 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.

↑