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

Gelatin For Specimen Adhesion

21 CFR 864.4010 / Pathology
FDA source (opens on fda.gov)

IFZ is the FDA product code for Gelatin For Specimen Adhesion, a class I device type, regulated under 21 CFR 864.4010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
IFZ
Device name
Gelatin For Specimen Adhesion
Regulation
21 CFR 864.4010
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
0

Clearances, product code IFZ

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

Applicants with the most clearances

Product code IFZ
Applicants holding the most 510(k) clearances under product code IFZ
ApplicantClearances
Surgipath Medical Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code