ROBIN CORDLESS HANDPIECE— 510(k) K832063

Substantially Equivalent

Kaycor Intl., Ltd.

FDA 510(k) clearance K832063 for ROBIN CORDLESS HANDPIECE, Substantially Equivalent on 1983-08-26. Applicant: Kaycor Intl., Ltd.. Device class: 1.

Clearance details

Applicant: Kaycor Intl., Ltd.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 1983-06-27
Decision date: 1983-08-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Kaycor Intl., Ltd.

K965072 — PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT1997-01-27
K931717 — YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAY1993-09-20
K822740 — K30000 DENTAL CHAIR1982-09-28
K813348 — YOSHIDA RIDO-F, MODEL LM-011982-01-07
K811210 — YOSHIDA-PANOURA 101981-08-24

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