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)

SPONGE, LAPAROTOMY GAUZE

K-Number: K760113 · 1976-07-15

ApplicantParke-Davis Co.
Decision Date1976-07-15
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

SPONGE, LAPAROTOMY GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1976-07-15 under 510(k) number K760113. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPONGE, LAPAROTOMY GAUZE?

SPONGE, LAPAROTOMY GAUZE is a medical device that received FDA 510(k) clearance on 1976-07-15. The listed applicant is Parke-Davis Co.. The 510(k) number is K760113.

When did SPONGE, LAPAROTOMY GAUZE receive FDA 510(k) clearance?

SPONGE, LAPAROTOMY GAUZE received FDA 510(k) clearance on 1976-07-15, under 510(k) number K760113.

Who is the listed applicant for SPONGE, LAPAROTOMY GAUZE?

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

What is the FDA product code for SPONGE, LAPAROTOMY GAUZE?

The FDA product code for SPONGE, LAPAROTOMY GAUZE 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 Parke-Davis 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.

K861725INTRACATH INTRAVENOUS CATHETER PLACEMENT UNITK862119DESERET FLO-THRU INJECTATE TEMPERATURE SENSORK855120ATI DISPOSABLE BIOLOGICAL TEST PACKK860570ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICEK860290VIAPIC CENTRAL LINE CATHETERK852192DISPOSABLE STEAM BIOLOGICAL TEST PACK

View all 47 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.

↑