Disposable Intravenous Hyperalimentation Bags

FDA 510(k) K863040 · Cher Mel Corp.

Substantially Equivalent

510(k) numberK863040

Submission

Device name
Disposable Intravenous Hyperalimentation Bags
Applicant
Cher Mel Corp.
Seattle, WA, US
Received
August 12, 1986
Decision date
October 31, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KPE – Container, I.V.
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5025
Specialty
General Hospital

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More from Gilero, LLC

510(k)DeviceDecision
K851516Chermel Scalp Vein SetFPA · Traditional 08/23/1985SE
K843324Sprague RAPPAPORT/SH-6008 Dispos. StethLDE · Traditional 06/06/1985SE
K842203Littman Type SH-6010, Nurse TypeLDE · Traditional 06/06/1985SE
K842824Chermel Bone ChiselsKDG · Traditional 08/02/1984SE
K842823Chermel OsteotomesGFI · Traditional 08/02/1984SE
K842822Chermel Bone GougesGDH · Traditional 08/02/1984SE

Questions and answers

When was Disposable Intravenous Hyperalimentation Bags cleared by the FDA?

Disposable Intravenous Hyperalimentation Bags (K863040) received a 510(k) decision of Substantially Equivalent on October 31, 1986, 80 days after the submission was received.

What is the product code of K863040?

The FDA product code is KPE – Container, I.V., a Class II (moderate risk) device regulated under 21 CFR 880.5025.