PATIENT TUBING HYTREL SIEMENS-ELEMA— 510(k) K841657

Name: FDA 510(k) clearance K841657
Creator: U.S. Food and Drug Administration
Published: 1984-05-23

Substantially Equivalent

Siemens Elema AB

FDA 510(k) clearance K841657 for PATIENT TUBING HYTREL SIEMENS-ELEMA, Substantially Equivalent on 1984-05-23. Applicant: Siemens Elema AB. Device class: 1.

Clearance details

Applicant: Siemens Elema AB
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1984-04-23
Decision date: 1984-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K952011 — PRIMA BREATHING BAGS1995-05-22
K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

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K002137 — CATHCOR DESKTOP2000-10-05
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