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)

BASIN, RECTANGULAR WASH

K-Number: K760495 · 1976-11-12

ApplicantLandmark Plastics
Decision Date1976-11-12
Product CodeFNY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BASIN, RECTANGULAR WASH is the device name listed in this FDA 510(k) record. The listed applicant is Landmark Plastics. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760495. The device is classified under product code FNY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASIN, RECTANGULAR WASH?

BASIN, RECTANGULAR WASH is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Landmark Plastics. The 510(k) number is K760495.

When did BASIN, RECTANGULAR WASH receive FDA 510(k) clearance?

BASIN, RECTANGULAR WASH received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760495.

Who is the listed applicant for BASIN, RECTANGULAR WASH?

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

What is the FDA product code for BASIN, RECTANGULAR WASH?

The FDA product code for BASIN, RECTANGULAR WASH is FNY.

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 Landmark Plastics 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.

K760548CARAFE AND LINERK760493DISH, SOAPK760490BEDPAN, GENERAL MEDICAL MEDI-PAKK760494BASIN, ROUND WASHK760492BASIN, LARGE OR SMALLK760496CUP, DISPOSABLE SPECIMEN

View all 13 devices →

Related Devices (Code: FNY)

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.

K832826AAP DOSIMETRY RELEASE OR BASIN SETSAmerican Hospital Supply Corp.K802538BASIN PACKTexas Medical Products, Inc.K800440STERILE SPONGE BOWLSPremium Plastics, Inc.K792625STERILIZATION PROCESS/PLACENTA BASINProcter & Gamble Mfg. Co.K7717338 EMESIS BASINBemis Health CareK760494BASIN, ROUND WASHLandmark Plastics

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.

↑