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

OXYGEN CONNECTING TUBES

K Number: K800504 · Decision Mar 18, 1980
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
61
Applicant Total
9
Review Days
14

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Basic Information

Device Name
OXYGEN CONNECTING TUBES
K Number
K800504
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Medi-Craft , Ltd.
Date Received
March 4, 1980
Decision Date
March 18, 1980
Product Code
BYX
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
BYX Tubing, Pressure And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BYX), 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
K800510 RECTAL & HARRIS FLUSH TUBES
K800505 URETHRAL CATHETER
K800507 FEEDING TUBES
K800509 CONNECTING TUBES
K800506 OXYGEN CATHETER
K800503 SUCTION CATHETER