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

Pipette, Pasteur

21 CFR 864.6160 / Hematology
FDA source (opens on fda.gov)

GJW is the FDA product code for Pipette, Pasteur, a class I device type, regulated under 21 CFR 864.6160. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GJW
Device name
Pipette, Pasteur
Regulation
21 CFR 864.6160
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
4
Ingested recalls
0

Clearances, product code GJW

By decision year
4 clearances under product code GJW with a decision year between 1976 and 1990, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code GJW by decision year
YearClearances
19761
19772
19901

Applicants with the most clearances

Product code GJW
Applicants holding the most 510(k) clearances under product code GJW
ApplicantClearances
Dade, Baxter Travenol Diagnostics, Inc.2
BD Becton Dickinson Vacutainer Systems Preanalytic1
Helena Laboratories, Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 27 companies shown, in name order