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

CANNULA, NASAL, OXYGEN

K Number: K781415 · Decision Sep 7, 1978
Classifications
1
FEI Numbers
263
Registration Numbers
263
Same Product Code
41
Applicant Total
4
Review Days
23

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Basic Information

Device Name
CANNULA, NASAL, OXYGEN
K Number
K781415
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5340
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vitalab Products Corp.
Date Received
August 15, 1978
Decision Date
September 7, 1978
Product Code
CAT
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
CAT Cannula, Nasal, Oxygen

Similar 510(k) Clearances

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

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Other Clearances by Vitalab Products Corp.

K Number Device Name
K781416 TUBING, FLEXIBLE, MEDICAL GAS
K781414 MASK, OXYGEN, NONBREATHING
K781413 MASK, PXYGEN