510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
KSLClass I

Solution, Copper Sulfate For Specific Gravity Determinations

21 CFR 864.9320 / Hematology
FDA source (opens on fda.gov)

KSL is the FDA product code for Solution, Copper Sulfate For Specific Gravity Determinations, a class I device type, regulated under 21 CFR 864.9320. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KSL
Device name
Solution, Copper Sulfate For Specific Gravity Determinations
Regulation
21 CFR 864.9320
Device class
Class I
Review panel
Hematology
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
0

Clearances, product code KSL

By decision year
2 clearances under product code KSL with a decision year between 1981 and 1988, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KSL by decision year
YearClearances
19811
19881

Applicants with the most clearances

Product code KSL
Applicants holding the most 510(k) clearances under product code KSL
ApplicantClearances
Accra Laboratories, Inc.1
Portable Medical Laboratories, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code