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)

LAPET & LAPWALL LAPAROTOMY SPONGES

K-Number: K830271 · 1983-06-02

ApplicantRitmed, Inc.
Decision Date1983-06-02
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

LAPET & LAPWALL LAPAROTOMY SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Ritmed, Inc.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K830271. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPET & LAPWALL LAPAROTOMY SPONGES?

LAPET & LAPWALL LAPAROTOMY SPONGES is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Ritmed, Inc.. The 510(k) number is K830271.

When did LAPET & LAPWALL LAPAROTOMY SPONGES receive FDA 510(k) clearance?

LAPET & LAPWALL LAPAROTOMY SPONGES received FDA 510(k) clearance on 1983-06-02, under 510(k) number K830271.

Who is the listed applicant for LAPET & LAPWALL LAPAROTOMY SPONGES?

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

What is the FDA product code for LAPET & LAPWALL LAPAROTOMY SPONGES?

The FDA product code for LAPET & LAPWALL LAPAROTOMY 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 Ritmed, 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.

K833626FLORET FOAM PREP SPONGEK832874ISOVIS WOUND PROTECTORK830270ISOVIS WOUND PROTECTORK830261FLORET STRUNG GAUZE SPONGESK830268FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMINK830266FLORET KITTNER OR K DISSECTOR

View all 22 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.

↑