VENOUS OXYGEN PROBE— 510(k) K811071

Substantially Equivalent

G.D. Searle and Co.

FDA 510(k) clearance K811071 for VENOUS OXYGEN PROBE, Substantially Equivalent on 1981-05-05. Applicant: G.D. Searle and Co.. Device class: 2.

Clearance details

Applicant: G.D. Searle and Co.
Product code: Code CCE
Device class: Class 2
Regulation: 21 CFR 868.1200
Advisory panel: Anesthesiology
Date received: 1981-04-20
Decision date: 1981-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K896311 — OPTEX BLOOD GAS MONITORING SYSTEM1990-01-03

More clearances from G.D. Searle and Co.

K821159 — IN-LINE OXYGEN MONITORING SYSTEM1982-05-25
K811068 — BYPASS COIL1981-05-27
K803238 — INTRAVASCULAR CATHETER1981-04-23
K810630 — SILICONE ELASTOMER COATED LATEX FOLEY1981-03-31
K810131 — ADMINISTRATION SET1981-02-26

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