INFUSION PUMP— 510(k) K831953

Substantially Equivalent

Cryosan, Inc.

FDA 510(k) clearance K831953 for INFUSION PUMP, Substantially Equivalent on 1983-07-19. Applicant: Cryosan, Inc.. Device class: 2.

Clearance details

Applicant: Cryosan, Inc.
Product code: Code FIR
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1983-06-15
Decision date: 1983-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FIR

K961137 — ATI PLASMA PUMP (PP-04)1996-06-14
K830818 — ASAHI BLOOD/PLASMA PUMP #ABP-01A &1983-04-12
K821139 — SPS-SINGLE PATIENT SYSTEM1982-05-10
K780410 — BLOOD PUMP-MODE S10K1978-05-03
K771705 — RS-7800 MINIPUMP1977-10-04

More clearances from Cryosan, Inc.

K830831 — AUTOMATED BLOOD CELL SEPARATOR1983-06-16
K822521 — AUTOMATED BLOOD CELL SEPARATOR1982-09-30
K813489 — ROCKING/CIRCULATING CYTO-THERM II 35701982-03-04
K812309 — CRYOSAN NORMAL SALINE1981-09-16
K812311 — CIRCULATING CYTO-THERMS1981-09-16

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