PREBYPASS FILTER— 510(k) K780485

Substantially Equivalent

Delta Medical Industries

FDA 510(k) clearance K780485 for PREBYPASS FILTER, Substantially Equivalent on 1978-04-05. Applicant: Delta Medical Industries. Device class: 2.

Clearance details

Applicant: Delta Medical Industries
Product code: Code KRJ
Device class: Class 2
Regulation: 21 CFR 870.4280
Advisory panel: Cardiovascular
Date received: 1978-03-27
Decision date: 1978-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KRJ

K990276 — POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER1999-10-01
K982385 — POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER1999-02-01
K940126 — AVECOR PRE-BYPASS FILTER1994-06-28
K900672 — PREBYPASS FILTER, CAT. NO. FPB-51990-04-03
K885154 — INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM1989-02-22

More clearances from Delta Medical Industries

K833884 — ISOTEC DISPOS. PRESSURE TRANSDUCER1984-04-17
K840253 — ONE-WAY AIR VALVE1984-04-05
K832470 — INFUSION PUMP1984-02-28
K830389 — ACCU-RYNGE PUMP SP-2501983-09-12
K831750 — PM-31983-07-26

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