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

Dna Probe, Yeast

21 CFR 866.2660 / Microbiology
FDA source (opens on fda.gov)

MLA is the FDA product code for Dna Probe, Yeast, a class I device type, regulated under 21 CFR 866.2660. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
MLA
Device name
Dna Probe, Yeast
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
2

Clearances, product code MLA

By decision year
2 clearances under product code MLA with a decision year between 1993 and 1993, 1993 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MLA by decision year
YearClearances
19932

Applicants with the most clearances

Product code MLA
Applicants holding the most 510(k) clearances under product code MLA
ApplicantClearances
Microprobe Corp.2

Companies listing this code with FDA

Companies whose registered establishments list this code