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 PH & PRESSURE ESOPHAGEAL MONIT

K-Number: K842690 · 1984-11-08

ApplicantSynectics AB
Decision Date1984-11-08
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT is the device name listed in this FDA 510(k) record. The listed applicant is Synectics AB. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K842690. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT?

SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Synectics AB. The 510(k) number is K842690.

When did SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT receive FDA 510(k) clearance?

SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT received FDA 510(k) clearance on 1984-11-08, under 510(k) number K842690.

Who is the listed applicant for SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT?

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

What is the FDA product code for SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT?

The FDA product code for SYNECTICS PH & PRESSURE ESOPHAGEAL MONIT is FFT.

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

Related Devices (Code: FFT)

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.

K102543BRAVO PH MONITORING SYSTEM AND ACCESSORIESGiven Imaging , Ltd.K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBESandhill Scientific, Inc.K002028BRAVO PH MONITORING SYSTEMEndonetics, Inc.K961346PH ANALYSIS MODULESynectics-DantecK950087LOT 440Medical Instruments Corporation Mic AGK955018TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATORInstrumentarium Corp.

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.

↑