MEDIBLEND (TM) LUNG DIFFUSION GAS MIXTURES— 510(k) K882210

Name: FDA 510(k) clearance K882210
Creator: U.S. Food and Drug Administration
Published: 1988-06-21

Substantially Equivalent

Linde Div. Union Carbide Corp.

FDA 510(k) clearance K882210 for MEDIBLEND (TM) LUNG DIFFUSION GAS MIXTURES, Substantially Equivalent on 1988-06-21. Applicant: Linde Div. Union Carbide Corp.. Device class: 1.

Clearance details

Applicant: Linde Div. Union Carbide Corp.
Product code: Code BXK
Device class: Class 1
Regulation: 21 CFR 868.6400
Advisory panel: Anesthesiology
Date received: 1988-05-26
Decision date: 1988-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXK

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K954803 — BLOOD GAS MIXTURES1996-01-25
K954804 — LUNG DIFFUSION MIXTURES1996-01-25
K954542 — LUNG DIFFUSION MIXTURE1995-12-22
K952838 — MEDICAL MIXTURE-LUNG DIFFUSION GAS MIXTURES1995-09-19
K953934 — MED-TECH LUNG DIFFUSION MIXTURE1995-09-18

More clearances from Linde Div. Union Carbide Corp.

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K882208 — MEDIBLEND (TM) MEDICAL LASER GAS MIXTURES1988-08-03
K882209 — MEDIBLEND (TM) CLINICAL BLOOD GAS MIXTURES1988-08-02
K832143 — MARK III OXYGEN WALKER SYS. RESERVOIR1983-08-26
K823582 — OXYGEN CONCENTRATOR UCC-1001983-01-05
K821841 — MEDIGAS SUCTION/DRAINAGE EQUIPMENT1982-07-02

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