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

Apparatus, General Use, Thin Layer Chromatography

21 CFR 862.2270 / Clinical Chemistry
FDA source (opens on fda.gov)

DPA is the FDA product code for Apparatus, General Use, Thin Layer Chromatography, a class I device type, regulated under 21 CFR 862.2270. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DPA
Device name
Apparatus, General Use, Thin Layer Chromatography
Regulation
21 CFR 862.2270
Device class
Class I
Review panel
Clinical Chemistry
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 DPA

By decision year
5 clearances under product code DPA with a decision year between 1976 and 1991, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DPA by decision year
YearClearances
19761
19771
19791
19891
19911

Applicants with the most clearances

Product code DPA
Applicants holding the most 510(k) clearances under product code DPA
ApplicantClearances
Ackerman Nuclear, Inc.1
Dyna-Tek Industries1
G.D. Searle and Co.1
Gelman Sciences, Inc.1
Technicon Instruments Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code