VENTIBOX— 510(k) K844160

Substantially Equivalent

Syncor Intl. Corp.

FDA 510(k) clearance K844160 for VENTIBOX, Substantially Equivalent on 1984-12-17. Applicant: Syncor Intl. Corp.. Device class: 1.

Clearance details

Applicant: Syncor Intl. Corp.
Product code: Code KPY
Device class: Class 1
Regulation: 21 CFR 892.6500
Advisory panel: Radiology
Date received: 1984-10-24
Decision date: 1984-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sylmar, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPY

K110900 — DISPOSABLE THYROID COLLAR2011-06-24
K962622 — INTRA-ORAL THERMOPLASTIC SHIELD1996-10-01
K954456 — THERMOPLASTIC SHIELD1995-12-21
K954146 — UTK-DTE AUTILARY SHIELD1995-12-06
K953610 — AUKULYTE1995-09-26

More clearances from Syncor Intl. Corp.

K945825 — SECURE SAFETY INSERT1995-04-10
K851828 — IRRADIATOR FOR BIOLOGICAL MATERIALS IBL-437-C1985-09-19
K850433 — CESIUM 137 ENDOMETRIAL SOURCE1985-08-21
K852023 — CESIUM 137 SOURCE, CSM-4, CSM-11, CSM-411985-08-21
K852665 — SYNCOR TRICH DIRECT IMMUNOFLUORESCENCE ASSAY1985-08-13

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