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)

GUAZE SPONGES

K-Number: K874067 · 1987-12-14

ApplicantInterpro Intl., Inc.
Decision Date1987-12-14
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

GUAZE SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Interpro Intl., Inc.. It received FDA 510(k) clearance on 1987-12-14 under 510(k) number K874067. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUAZE SPONGES?

GUAZE SPONGES is a medical device that received FDA 510(k) clearance on 1987-12-14. The listed applicant is Interpro Intl., Inc.. The 510(k) number is K874067.

When did GUAZE SPONGES receive FDA 510(k) clearance?

GUAZE SPONGES received FDA 510(k) clearance on 1987-12-14, under 510(k) number K874067.

Who is the listed applicant for GUAZE SPONGES?

The FDA 510(k) record lists Interpro Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GUAZE SPONGES?

The FDA product code for GUAZE SPONGES 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 Interpro Intl., 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.

K890968VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)K891642PATIENT EXAMINATION GLOVES (LATEX)K890891LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)K891440PATIENT EXAMINATION GLOVES (LATEX)K891438PATIENT EXAMINATION GLOVES (LATEX)K881374SURGEONS GLOVES

View all 11 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.

↑