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

Dispensers, Paraffin

21 CFR 864.3010 / Pathology
FDA source (opens on fda.gov)

IDW is the FDA product code for Dispensers, Paraffin, a class I device type, regulated under 21 CFR 864.3010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
IDW
Device name
Dispensers, Paraffin
Regulation
21 CFR 864.3010
Device class
Class I
Review panel
Pathology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
1

Clearances, product code IDW

By decision year
1 clearance under product code IDW with a decision year between 1979 and 1979, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IDW by decision year
YearClearances
19791

Applicants with the most clearances

Product code IDW
Applicants holding the most 510(k) clearances under product code IDW
ApplicantClearances
Thermolyne Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 30 companies shown, in name order