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

Micro Pipette

21 CFR 862.2050 / Clinical Chemistry
FDA source (opens on fda.gov)

JRC is the FDA product code for Micro Pipette, a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
JRC
Device name
Micro Pipette
Regulation
21 CFR 862.2050
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
6
Ingested recalls
3

Clearances, product code JRC

By decision year
6 clearances under product code JRC with a decision year between 1976 and 1984, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code JRC by decision year
YearClearances
19761
19771
19801
19821
19842

Applicants with the most clearances

Product code JRC
Applicants holding the most 510(k) clearances under product code JRC
ApplicantClearances
Abco Dealers, Inc.1
American Dade1
Meridian Diagnostics, Inc.1
Scientific Manufacturing Industries1
Sherwood Medical Industries1
Vitex1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 86 companies shown, in name order