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)

DRENOVAC

K-Number: K883982 · 1989-02-23

ApplicantIberhospitex, S.A.
Decision Date1989-02-23
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DRENOVAC is the device name listed in this FDA 510(k) record. The listed applicant is Iberhospitex, S.A.. It received FDA 510(k) clearance on 1989-02-23 under 510(k) number K883982. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRENOVAC?

DRENOVAC is a medical device that received FDA 510(k) clearance on 1989-02-23. The listed applicant is Iberhospitex, S.A.. The 510(k) number is K883982.

When did DRENOVAC receive FDA 510(k) clearance?

DRENOVAC received FDA 510(k) clearance on 1989-02-23, under 510(k) number K883982.

Who is the listed applicant for DRENOVAC?

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

What is the FDA product code for DRENOVAC?

The FDA product code for DRENOVAC is GCY.

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 Iberhospitex, S.A. 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.

K883983SANIFIXK881936OPER-FILM-ADHESIVE MEMBRANE

Related Devices (Code: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, 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.

↑