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FDA 510(k)

SANIFIX

K-Number: K883983 · 1988-12-13

ApplicantIberhospitex, S.A.
Decision Date1988-12-13
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

SANIFIX 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 1988-12-13 under 510(k) number K883983. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SANIFIX?

SANIFIX is a medical device that received FDA 510(k) clearance on 1988-12-13. The listed applicant is Iberhospitex, S.A.. The 510(k) number is K883983.

When did SANIFIX receive FDA 510(k) clearance?

SANIFIX received FDA 510(k) clearance on 1988-12-13, under 510(k) number K883983.

Who is the listed applicant for SANIFIX?

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 SANIFIX?

The FDA product code for SANIFIX is KGX.

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.

K883982DRENOVACK881936OPER-FILM-ADHESIVE MEMBRANE

Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer 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.

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