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)

SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM

K-Number: K904625 · 1991-08-20

ApplicantSynectics-Dantec
Decision Date1991-08-20
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Synectics-Dantec. It received FDA 510(k) clearance on 1991-08-20 under 510(k) number K904625. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM?

SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM is a medical device that received FDA 510(k) clearance on 1991-08-20. The listed applicant is Synectics-Dantec. The 510(k) number is K904625.

When did SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM receive FDA 510(k) clearance?

SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM received FDA 510(k) clearance on 1991-08-20, under 510(k) number K904625.

Who is the listed applicant for SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM?

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

What is the FDA product code for SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM?

The FDA product code for SYNECTICS LIBERTY SYSTEM, PC POLYGRAF AND POLYGRAM is BZG.

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 Synectics-Dantec 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.

K961346PH ANALYSIS MODULEK925405ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF.K924875MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONSK914793MONOCRYSTANT PH/LES CATHETER, MODIFICATIONK924383SYNECTICS LIBERTY SYSTEM, PC POLYGRAF/POLYGRAM UROK913817MONOCRYSTANT PH-REFERENCE CATHETER, MODIFICATION

View all 19 devices →

Related Devices (Code: BZG)

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.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

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.

↑