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)

CLEAN-SORB

K-Number: K941099 · 1994-09-30

ApplicantHospital Specialty Co.
Decision Date1994-09-30
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

CLEAN-SORB is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Specialty Co.. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K941099. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAN-SORB?

CLEAN-SORB is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Hospital Specialty Co.. The 510(k) number is K941099.

When did CLEAN-SORB receive FDA 510(k) clearance?

CLEAN-SORB received FDA 510(k) clearance on 1994-09-30, under 510(k) number K941099.

Who is the listed applicant for CLEAN-SORB?

The FDA 510(k) record lists Hospital Specialty Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEAN-SORB?

The FDA product code for CLEAN-SORB is EFQ.

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 Hospital Specialty Co. 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.

K990861WOUND DRESSING/ABD PAD, MODEL #10810K882094GARDS DEODORANT SANITARY NAPKINK880454AT EASE STRESS PADK880455AT EASE ADULT DIAPERK822242SANITARY/OB NAPKINSK822433GARDS (UNSCENTED, MENSTRUAL PAD)

View all 7 devices →

Related Devices (Code: EFQ)

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.

K991757NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILEFurlong IndustriesK991215SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'SSymtex Healthcare Corp.K990974VITOP DRESSINGWonder & Bioenergy Hi-Tech America, Inc.K990584GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLEBroadline Medical IndustriesK984187CROSSTEX NON-WOVEN SPONGESCrosstex Intl.K983016GAUZE, SPONGES, CAT # 11-003Vitalcare Group, 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.

↑