Carafe, Personal, 1-QT Semi-Rectangular

FDA 510(k) K760072 · Bemis Health Care

Substantially Equivalent

510(k) numberK760072

Submission

Device name
Carafe, Personal, 1-QT Semi-Rectangular
Applicant
Bemis Health Care
Mchenry, IL, US
Received
June 18, 1976
Decision date
July 20, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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Questions and answers

When was Carafe, Personal, 1-QT Semi-Rectangular cleared by the FDA?

Carafe, Personal, 1-QT Semi-Rectangular (K760072) received a 510(k) decision of Substantially Equivalent on July 20, 1976, 32 days after the submission was received.