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

Microtome, Cryostat

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

IDP is the FDA product code for Microtome, Cryostat, 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 10 recalls.

Classification record

Product code
IDP
Device name
Microtome, Cryostat
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
10

Clearances, product code IDP

By decision year
1 clearance under product code IDP with a decision year between 1988 and 1988, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IDP by decision year
YearClearances
19881

Applicants with the most clearances

Product code IDP
Applicants holding the most 510(k) clearances under product code IDP
ApplicantClearances
Exakt Medical Instruments, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 21 companies shown, in name order