Accu-Rynge Insulin Pump #SP-250

FDA 510(k) K820482 · Delta Medical Industries

Substantially Equivalent

510(k) numberK820482

Submission

Device name
Accu-Rynge Insulin Pump #SP-250
Applicant
Delta Medical Industries
Mchenry, IL, US
Received
February 22, 1982
Decision date
March 26, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FRN – Pump, Infusion
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

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Questions and answers

When was Accu-Rynge Insulin Pump #SP-250 cleared by the FDA?

Accu-Rynge Insulin Pump #SP-250 (K820482) received a 510(k) decision of Substantially Equivalent on March 26, 1982, 32 days after the submission was received.

What is the product code of K820482?

The FDA product code is FRN – Pump, Infusion, a Class II (moderate risk) device regulated under 21 CFR 880.5725.