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

Bath, Incubators/Water, All

21 CFR 866.2540 / Microbiology
FDA source (opens on fda.gov)

JTQ is the FDA product code for Bath, Incubators/Water, All, a class I device type, regulated under 21 CFR 866.2540. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and 11 recalls.

Classification record

Product code
JTQ
Device name
Bath, Incubators/Water, All
Regulation
21 CFR 866.2540
Device class
Class I
Review panel
Microbiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
12
Ingested recalls
11

Clearances, product code JTQ

By decision year
12 clearances under product code JTQ with a decision year between 1977 and 1988, 1983 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code JTQ by decision year
YearClearances
19771
19791
19801
19812
19821
19834
19851
19881

Applicants with the most clearances

Product code JTQ
Applicants holding the most 510(k) clearances under product code JTQ
ApplicantClearances
Bionetic Laboratory Products2
Boekel Industries, Inc.2
Flow Laboratories, Inc.1
Forma Scientific, Inc.1
Mdt Corp., Inc.1
Remel Co.1
Scientific Sales Intl., Inc.1
Sterling Drug, Inc.1
Sybron Corp.1
Thermolyne Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 51 companies shown, in name order