Profile General Set Assayed Serum Contr

FDA 510(k) K820468 · General Diagnostics

Substantially Equivalent

510(k) numberK820468

Submission

Device name
Profile General Set Assayed Serum Contr
Applicant
General Diagnostics
Mchenry, IL, US
Received
February 22, 1982
Decision date
March 25, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DIF – Drug Mixture Control Materials
Device class
Class I (low risk)
Regulation
21 CFR 862.3280
Specialty
Clinical Toxicology

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K833709Ceftizoxime 30 MCG Antimicrobial DiskJTN · Traditional 12/30/1983SE
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Questions and answers

When was Profile General Set Assayed Serum Contr cleared by the FDA?

Profile General Set Assayed Serum Contr (K820468) received a 510(k) decision of Substantially Equivalent on March 25, 1982, 31 days after the submission was received.

What is the product code of K820468?

The FDA product code is DIF – Drug Mixture Control Materials, a Class I (low risk) device regulated under 21 CFR 862.3280.