FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ENDOTRACHEAL TUBE

K Number: K781339 · Decision Aug 15, 1978
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
3
Review Days
12

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Basic Information

Device Name
ENDOTRACHEAL TUBE
K Number
K781339
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Life-Line Products, Inc.
Date Received
August 3, 1978
Decision Date
August 15, 1978
Product Code
BTR
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
BTR Tube, Tracheal (W/Wo Connector)

Similar 510(k) Clearances

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

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Other Clearances by Life-Line Products, Inc.

K Number Device Name
K821456 ENDOTRACHEAL TUBE
K821243 ENDOTRACHEAL TUBE