DERMTRODE— 510(k) K883869

Substantially Equivalent

World Precision Instruments, Inc.

FDA 510(k) clearance K883869 for DERMTRODE, Substantially Equivalent on 1988-09-30. Applicant: World Precision Instruments, Inc.. Device class: 1.

Clearance details

Applicant: World Precision Instruments, Inc.
Product code: Code GYA
Device class: Class 1
Regulation: 21 CFR 882.1410
Advisory panel: Neurology
Date received: 1988-09-13
Decision date: 1988-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Haven, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GYA

K854396 — RUB E-Z1986-05-08
K830877 — AP-CHECK1983-06-08
K820040 — SC-IT IMPEDANCE TESTER1982-01-28
K781475 — ELECTRODE IMPEDANCE TESTER-MODEL 5001978-09-07

More clearances from World Precision Instruments, Inc.

K852289 — MODEL SA3 ESOPHAGEAL PH ELECTRODE1985-07-25

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