510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K133522Substantially Equivalent

Rightest Diabetes Management Software and Adapter (Existing Cleared K113007),rightest New Adapters-3,Ge Diabetes Managem

Bionime Coporation, Mission Viejo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K133522 is the FDA 510(k) clearance record for RIGHTEST DIABETES MANAGEMENT SOFTWARE AND ADAPTER (EXISTING CLEARED K113007),RIGHTEST NEW ADAPTERS-3,GE DIABETES MANAGEM, a class II device, cleared for Bionime Coporation on under FDA product code NBW (System, Test, Blood Glucose, Over The Counter). FDA records list 3 510(k) clearances for Bionime Coporation, from to . As of , FDA records show no recalls naming K133522.

Clearance record

Decision date
Received
(153 days to decision)
Product code
NBW System, Test, Blood Glucose, Over The Counter
Regulation
21 CFR 862.1345
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Bionime Coporation 2700 La Paz Rd., Mission Viejo CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NBW

Trailing 12 months
2 clearances under product code NBW in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NBW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260