FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SUCTION CATHETER

K Number: K800503 · Decision Mar 18, 1980
Classifications
1
FEI Numbers
257
Registration Numbers
257
Same Product Code
115
Applicant Total
9
Review Days
14

Basic Information

Device Name
SUCTION CATHETER
K Number
K800503
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
MEDI-CRAFT LTD.
Date Received
March 4, 1980
Decision Date
March 18, 1980
Product Code
BSY
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BSY Catheters, Suction, Tracheobronchial

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BSY), ordered by most recent decision date.

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Other Clearances by MEDI-CRAFT LTD.

K Number Device Name
K861949 SUCTION CATHETER KIT
K800508 STOMACH TUBES
K800505 URETHRAL CATHETER
K800507 FEEDING TUBES
K800510 RECTAL & HARRIS FLUSH TUBES
K800509 CONNECTING TUBES
K800506 OXYGEN CATHETER
K800504 OXYGEN CONNECTING TUBES