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)

GOAL TENDER

K-Number: K832878 · 1983-10-14

ApplicantDna Medical, Inc.
Decision Date1983-10-14
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GOAL TENDER is the device name listed in this FDA 510(k) record. The listed applicant is Dna Medical, Inc.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832878. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOAL TENDER?

GOAL TENDER is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Dna Medical, Inc.. The 510(k) number is K832878.

When did GOAL TENDER receive FDA 510(k) clearance?

GOAL TENDER received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832878.

Who is the listed applicant for GOAL TENDER?

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

What is the FDA product code for GOAL TENDER?

The FDA product code for GOAL TENDER is BWF.

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 Dna Medical, 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.

K833659IV EXTENSION SETK822891FLO CONTROLK821929SUBCLAVIANK820628J-CATHETER

Related Devices (Code: BWF)

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.

K241152InSeeTidal Medical Technologies, LLCK233855AllPEPEnchant Tek Co. , Ltd.K221058LungTrainer (MD2 & MD3)Lung Trainers, LLCK222018Breathe+Peep Medical, LLC Dba Go2 DevicesK220565Hudson RCI Triflo II Incentive Deep Breathing ExerciserMedline Industries, Inc.K203378PulsehalerRespinova, Ltd.

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.

↑