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

Bacillus Subtilis Microbiology Assay, Tobramycin

21 CFR 862.3900 / Clinical Toxicology
FDA source (opens on fda.gov)

DID is the FDA product code for Bacillus Subtilis Microbiology Assay, Tobramycin, a class II device type, regulated under 21 CFR 862.3900. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DID
Device name
Bacillus Subtilis Microbiology Assay, Tobramycin
Regulation
21 CFR 862.3900
Device class
Class II
Review panel
Clinical Toxicology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
5
Ingested recalls
0

Clearances, product code DID

By decision year
5 clearances under product code DID with a decision year between 1978 and 1982, 1978 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code DID by decision year
YearClearances
19783
19801
19821

Applicants with the most clearances

Product code DID
Applicants holding the most 510(k) clearances under product code DID
ApplicantClearances
Beckman Instruments, Inc.1
Monitor Science Corp.1
New England Nuclear1
Nichols Institute Diagnostics1
Syva Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code DID.