510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K070334Substantially Equivalent

R&d Sickle Qc Control

R & D Systems, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K070334 is the FDA 510(k) clearance record for R&D SICKLE QC CONTROL, a class II device, cleared for R&D Systems, Inc. on under FDA product code GGM (Control, Hemoglobin). FDA records list 79 510(k) clearances for R&D Systems, Inc., from to . As of , FDA records show no recalls naming K070334.

Clearance record

Decision date
Received
(52 days to decision)
Product code
GGM Control, Hemoglobin
Regulation
21 CFR 864.8625
Device class
Class II
Review panel
Hematology
Applicant
R&D Systems, Inc. 614 Mckinley Pl. NE, Minneapolis MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GGM

Trailing 12 months

FDA records hold no clearances under product code GGM in the trailing twelve months.

FDA records show no clearances under product code GGM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GGM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260