Atlas FDA

JTQ

12 FDA 510(k) clearances · Product code

34 daysmedian time to decision
56 days90th percentile
12clearances measured

FDA profile

Official device name
Bath, Incubators/Water, All
Device class
Class I (low risk)
Regulation
21 CFR 866.2540
Medical specialty
Microbiology
Flags
GMP exempt
Adverse events (MAUDE)
1994: 1 · 1998: 1 · 2006: 3 · 2007: 4
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER (K875275)Sterling Drug, Inc.1988-01-27
PLATE INCUBATOR (K853379)Scientific Sales Intl., Inc.1985-09-03
ANHYDRIC INCUBATORS, CULTURE INCUBATOR (K831592)Boekel Industries, Inc.1983-06-16
C.A.T. REAGENT KIT (K830322)Remel Co.1983-03-28
AUTOMATED ELISA READER LBI 300 (K830227)Bionetic Laboratory Products1983-03-10
LBI-100 37DEGREES INCUBATOR (K830405)Bionetic Laboratory Products1983-03-10
WATER BATH (K822564)Boekel Industries, Inc.1982-09-14
FORMA CH/P GAS PROCESSOR (K812826)Forma Scientific, Inc.1981-10-23
TITERTEK MICROPLATE INCUBATOR (K812340)Flow Laboratories, Inc.1981-09-23
SPOR-O-THERM (K801462)Mdt Corp., Inc.1980-07-28
TEMPTRONIC 100 WATER BATH (K792060)Sybron Corp.1979-12-04
BLOOD BANK DRI-BATH (K760928)Thermolyne Corp.1977-01-10

Track JTQ automatically

Every clearance here is in the API, with alerts when new ones post.