510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771138Substantially Equivalent

Pipets Borosilicate Glass

Dade, Baxter Travenol Diagnostics, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771138 is the FDA 510(k) clearance record for PIPETS BOROSILICATE GLASS, a class I device, cleared for Dade, Baxter Travenol Diagnostics, Inc. on under FDA product code GJW (Pipette, Pasteur). FDA records list 44 510(k) clearances for Dade, Baxter Travenol Diagnostics, Inc., from to . As of , FDA records show no recalls naming K771138.

Clearance record

Decision date
Received
(41 days to decision)
Product code
GJW Pipette, Pasteur
Regulation
21 CFR 864.6160
Device class
Class I
Review panel
Hematology
Applicant
Dade, Baxter Travenol Diagnostics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GJW

Trailing 12 months

FDA records hold no clearances under product code GJW in the trailing twelve months.

FDA records show no clearances under product code GJW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GJW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260