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

Microtome, Accessories

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

IDL is the FDA product code for Microtome, Accessories, a class I device type, regulated under 21 CFR 864.3010. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IDL
Device name
Microtome, Accessories
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
5
Ingested recalls
0

Clearances, product code IDL

By decision year
5 clearances under product code IDL with a decision year between 1980 and 1986, 1983 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code IDL by decision year
YearClearances
19801
19811
19832
19861

Applicants with the most clearances

Product code IDL
Applicants holding the most 510(k) clearances under product code IDL
ApplicantClearances
Surgipath Medical Industries, Inc.2
American Optical Corp.1
Miles Laboratories, Inc.1
Polymer Technology Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 38 companies shown, in name order