Tma Bicarbonate Diluent

FDA 510(k) K771044 · Hyland Therapeutic Div., Travenol Laboratories

Substantially Equivalent

510(k) numberK771044

Submission

Device name
Tma Bicarbonate Diluent
Applicant
Hyland Therapeutic Div., Travenol Laboratories
Mchenry, IL, US
Received
June 10, 1977
Decision date
July 15, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJS – Controls For Blood-Gases, (Assayed And Unassayed)
Device class
Class I (low risk)
Regulation
21 CFR 862.1660
Specialty
Clinical Chemistry

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Questions and answers

When was Tma Bicarbonate Diluent cleared by the FDA?

Tma Bicarbonate Diluent (K771044) received a 510(k) decision of Substantially Equivalent on July 15, 1977, 35 days after the submission was received.

What is the product code of K771044?

The FDA product code is JJS – Controls For Blood-Gases, (Assayed And Unassayed), a Class I (low risk) device regulated under 21 CFR 862.1660.