ECHO-PULSE KM555— 510(k) K821736

Substantially Equivalent

Rabar, Inc.

FDA 510(k) clearance K821736 for ECHO-PULSE KM555, Substantially Equivalent on 1982-12-09. Applicant: Rabar, Inc.. Device class: 2.

Clearance details

Applicant: Rabar, Inc.
Product code: Code GXW
Device class: Class 2
Regulation: 21 CFR 882.1240
Advisory panel: Neurology
Date received: 1982-06-14
Decision date: 1982-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GXW

K921863 — SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS1992-09-28
K903085 — SMS-712NA1990-10-05
K853432 — 5.0 IOP & 7.5 IOP PROBES1986-02-07
K833522 — NEURO SECTOR FIXATION DEVICE1984-05-25
K770788 — ECHOENCEPHALOGRAPH, DIGITAL,DIGIECHO20001977-05-06

More clearances from Rabar, Inc.

K844017 — MICROTENS 7757 T.E.N.S. STIMULATOR1984-11-30
K842414 — ECHO PULSE BURST1984-07-27

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