Chromatography Clinical Use 75JQR
FDA 510(k) K914841 · Millipore Corp.
510(k) numberK914841
Submission
- Device name
- Chromatography Clinical Use 75JQR
- Applicant
- Millipore Corp.
Milford, MA, US - Received
- October 25, 1991
- Decision date
- December 10, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- KIE – Apparatus, High Pressure Liquid Chromatography
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2260
- Specialty
- Clinical Chemistry
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Questions and answers
When was Chromatography Clinical Use 75JQR cleared by the FDA?
Chromatography Clinical Use 75JQR (K914841) received a 510(k) decision of Substantially Equivalent on December 10, 1991, 46 days after the submission was received.
What is the product code of K914841?
The FDA product code is KIE – Apparatus, High Pressure Liquid Chromatography, a Class I (low risk) device regulated under 21 CFR 862.2260.