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)

SIL-MED WASTE FLUID DUMP BAG

K-Number: K891471 · 1989-08-15

ApplicantSil-Med Corp.
Decision Date1989-08-15
Product CodeKDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SIL-MED WASTE FLUID DUMP BAG is the device name listed in this FDA 510(k) record. The listed applicant is Sil-Med Corp.. It received FDA 510(k) clearance on 1989-08-15 under 510(k) number K891471. The device is classified under product code KDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIL-MED WASTE FLUID DUMP BAG?

SIL-MED WASTE FLUID DUMP BAG is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Sil-Med Corp.. The 510(k) number is K891471.

When did SIL-MED WASTE FLUID DUMP BAG receive FDA 510(k) clearance?

SIL-MED WASTE FLUID DUMP BAG received FDA 510(k) clearance on 1989-08-15, under 510(k) number K891471.

Who is the listed applicant for SIL-MED WASTE FLUID DUMP BAG?

The FDA 510(k) record lists Sil-Med Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIL-MED WASTE FLUID DUMP BAG?

The FDA product code for SIL-MED WASTE FLUID DUMP BAG is KDG.

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 Sil-Med Corp. 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.

K972521NAVIGATOR (STYLET) 2006K961392ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT IIK961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAINK961295SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCARK960099PENROSE DRAIN MODELS 6001 - 6007K955463GRIP-A-BOOTS

View all 29 devices →

Related Devices (Code: KDG)

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.

K952678STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KITAvail-Southwest DivisionK952200OMNI-JUGWaterstone Medical, Inc.K894785SURGICAL CHISEL/OSTEOTOMEFdt Precision Machine Co., Inc.K872947POREX QUALITY PLASTIC SURGERY INSTRUMENTSPorex MedicalK872092OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5Military Engineering, Inc.K842824CHERMEL BONE CHISELSCher Mel Corp.

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.

↑