Home / 510(k) Clearances / K896670

510(k) K896670

TIP TOP(R) DISPENSER CAPS by Helena Laboratories — Product Code GJW

K896670 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "TIP TOP(R) DISPENSER CAPS". The FDA issued a decision of Substantially Equivalent on March 23, 1990. The device falls under product code GJW (Pipette, Pasteur), a Class I device regulated under 21 CFR 864.6160. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 1990
Date Received
November 27, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pipette, Pasteur
Device Class
Class I
Regulation Number
864.6160
Review Panel
HE
Submission Type

Other clearances by Helena Laboratories

  • K213396 — SPIFE A1AT kit (October 13, 2022)
  • K192931 — V8 Nexus Hemoglobin Ultrascreen, V8 AFSA2 Hemo Control (April 19, 2022)
  • K131479 — V8 SP NORMAL CONTROL, ABNORMAL CONTROL (October 7, 2013)
  • K100103 — SPECIALTY ASSAYED CONTROL-2 (December 15, 2010)
  • K061991 — PLATELETWORKS ARACHIDONIC ACID, MODEL PW-ACA (February 23, 2007)
  • K061069 — SPIFE IFE-15 PENTAVALENT, MODEL 3456, SPIFE IFE-9 PENTAVALENT KIT, MODEL 3457, S (July 6, 2006)
  • K061014 — ACTALYKE QC KIT, MODELS AQC-HP AND AQC-LP (May 10, 2006)
  • K050053 — HEMORAM/AGGRAM ANALYZER (July 11, 2005)
  • K024162 — SPIFE 3000 TITAN GEL IGG IEF KIT, MODEL 3389 (February 19, 2003)
  • K023761 — PLATELETWORKS, MODELS PW-A, PW-C (February 14, 2003)

Other clearances for product code GJW

  • K771138 — PIPETS BOROSILICATE GLASS (August 4, 1977)
  • K771137 — PIPETS UNIFORM DROP SIZE BOROSILICATE (August 4, 1977)
  • K760899 — STERILE DISPOSABLE COTTON PLUGGED SER. (November 9, 1976)

FDA data resources