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)

TUBE-STRAP

K-Number: K791781 · 1979-09-19

ApplicantOlympic Medical Corp.
Decision Date1979-09-19
Product CodeJAY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TUBE-STRAP is the device name listed in this FDA 510(k) record. The listed applicant is Olympic Medical Corp.. It received FDA 510(k) clearance on 1979-09-19 under 510(k) number K791781. The device is classified under product code JAY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE-STRAP?

TUBE-STRAP is a medical device that received FDA 510(k) clearance on 1979-09-19. The listed applicant is Olympic Medical Corp.. The 510(k) number is K791781.

When did TUBE-STRAP receive FDA 510(k) clearance?

TUBE-STRAP received FDA 510(k) clearance on 1979-09-19, under 510(k) number K791781.

Who is the listed applicant for TUBE-STRAP?

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

What is the FDA product code for TUBE-STRAP?

The FDA product code for TUBE-STRAP is JAY.

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 Olympic Medical Corp. 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.

K081094OLYMPIC PASTEURMATIC, MODELS 3000 AND 3500K031149OLYMPIC CFM 6000K020335OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEM, MODEL 5330K001056OLYMPIC WARM-UPK983229OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEMK971601OLYMPIC BILI-BASSINET

View all 37 devices →

Related Devices (Code: JAY)

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.

K944988CUSTOM MEDICAL SUSPENSION STRAPCustom Medical Specialties, Inc.K873491BLOCK, BITE, INTUBATIONB&B Medical Technologies, Inc.K860583DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 1315Dale Medical Products, Inc.K850924JEE FRAME (VENTILATOR CIRCUIT SUPPORT)Vulcan Laboratories, Inc.K850309COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCKAckrad LaboratoriesK840844ENDO-SECUREExidyne, 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.

↑