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)

SIGNAL AVERAGER MODEL 4202

K-Number: K781290 · 1978-09-15

ApplicantPrinceton Applied Research Corp.
Decision Date1978-09-15
Product CodeGWK
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SIGNAL AVERAGER MODEL 4202 is the device name listed in this FDA 510(k) record. The listed applicant is Princeton Applied Research Corp.. It received FDA 510(k) clearance on 1978-09-15 under 510(k) number K781290. The device is classified under product code GWK. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGNAL AVERAGER MODEL 4202?

SIGNAL AVERAGER MODEL 4202 is a medical device that received FDA 510(k) clearance on 1978-09-15. The listed applicant is Princeton Applied Research Corp.. The 510(k) number is K781290.

When did SIGNAL AVERAGER MODEL 4202 receive FDA 510(k) clearance?

SIGNAL AVERAGER MODEL 4202 received FDA 510(k) clearance on 1978-09-15, under 510(k) number K781290.

Who is the listed applicant for SIGNAL AVERAGER MODEL 4202?

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

What is the FDA product code for SIGNAL AVERAGER MODEL 4202?

The FDA product code for SIGNAL AVERAGER MODEL 4202 is GWK.

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 Princeton Applied Research 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.

K781289PREAMPLIFIER MODEL 113

Related Devices (Code: GWK)

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.

K060919ACTICALRespironics, Inc.K061870VITALSENSE XHRRespironics, Inc.K052489ACTIHEARTRespironics, Inc.K991045MINI-LOGGER SERIES 2000Mini-Mitter Co., Inc.K905594NEUROFILE DATA STORAGE/ACCESORIES TO THE EEG-4300Nihon Kohden America, Inc.K904328VISTA POLYSOMNOGRAPHY COMPUTER SYSTEMTelediagnostic Systems, 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.

↑