510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K960058Substantially Equivalent

Oxitemp, 3301T Sa

Bci Intl., Inc., Waukesha WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960058 is the FDA 510(k) clearance record for OXITEMP, 3301T SA, a class II device, cleared for Bci Intl., Inc. on under FDA product code DQA (Oximeter). FDA records list 20 510(k) clearances for Bci Intl., Inc., from to . As of , FDA records show no recalls naming K960058.

Clearance record

Decision date
Received
(134 days to decision)
Product code
DQA Oximeter
Regulation
21 CFR 870.2700
Device class
Class II
Review panel
Cardiovascular
Applicant
Bci Intl., Inc. W238 N1650 Rockwood Dr., Waukesha WI
510(k) summary
Summary
Third party review
No

Clearances, product code DQA

Trailing 12 months
12 clearances under product code DQA in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQA, trailing twelve months
MonthClearances
November 20252
December 20253
January 20261
February 20262
March 20260
April 20261
May 20263
June 20260
July 20260
August 20260
September 20260
October 20260