Sterile Water & Saline in Plastic Btl.

FDA 510(k) K800753 · Travenol Laboratories, S.A.

Substantially Equivalent

510(k) numberK800753

Submission

Device name
Sterile Water & Saline in Plastic Btl.
Applicant
Travenol Laboratories, S.A.
Mchenry, IL, US
Received
April 4, 1980
Decision date
April 24, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTT – Humidifier, Respiratory Gas, (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5450
Specialty
Anesthesiology

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Questions and answers

When was Sterile Water & Saline in Plastic Btl. cleared by the FDA?

Sterile Water & Saline in Plastic Btl. (K800753) received a 510(k) decision of Substantially Equivalent on April 24, 1980, 20 days after the submission was received.

What is the product code of K800753?

The FDA product code is BTT – Humidifier, Respiratory Gas, (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5450.