MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS— 510(k) K924875

Name: FDA 510(k) clearance K924875
Creator: U.S. Food and Drug Administration
Published: 1994-06-30

Substantially Equivalent - Subject to Tracking Reg.

Synectics-Dantec

FDA 510(k) clearance K924875 for MICROTRAPPER/MICRODIGITRAPPER, ADD MODIFICATIONS, Substantially Equivalent - Subject to Tracking Reg. on 1994-06-30. Applicant: Synectics-Dantec. Device class: 2.

Clearance details

Applicant: Synectics-Dantec
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1992-09-14
Decision date: 1994-06-30
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Traditional
Location: Irving, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZQ

view all

K253274 — BedDot (G1)2026-06-25
K251326 — Respiration Rate algorithm2026-06-11
K250093 — Linshom Continuous Predictive Respiratory Monitoring System (CPRMS)2025-09-26
K250934 — Respiree Cardio- Respiratory Monitor System2025-08-05
K243183 — RTMsense Respiratory Monitoring System2025-06-27

More clearances from Synectics-Dantec

view all

K961346 — PH ANALYSIS MODULE1997-01-29
K925405 — ZINETICS COMPOSITE SENSOR PROBE W/INTERNAL REF.1994-09-30
K914793 — MONOCRYSTANT PH/LES CATHETER, MODIFICATION1993-12-13
K924383 — SYNECTICS LIBERTY SYSTEM, PC POLYGRAF/POLYGRAM URO1993-06-18
K913817 — MONOCRYSTANT PH-REFERENCE CATHETER, MODIFICATION1992-06-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.