Home / 510(k) Clearances / K970176

510(k) K970176

HCG CONTROLS by International Newtech Development, Inc. — Product Code JJX

K970176 is an FDA 510(k) premarket notification submitted by International Newtech Development, Inc. for the device "HCG CONTROLS". The FDA issued a decision of Substantially Equivalent on February 6, 1997. The device falls under product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. International Newtech Development, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 6, 1997
Date Received
January 17, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Single (Specified) Analyte Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type

Other clearances by International Newtech Development, Inc.

  • K993850 — URINALYSIS REAGENT STRIPS (10 PARAMETERS) (January 3, 2000)
  • K974060 — MINISTRIP/ SERUM AND URINE COMBO HCG TEST (April 9, 1998)
  • K974059 — ONE STEP MIDSTREAM HCG PREGNANCY TEST (April 9, 1998)
  • K974009 — PS-UNIT CASSETTE/SERUM AND URINE COMBO HCG (March 13, 1998)
  • K963133 — PS-UNIT CASSETTE/SERUM HCG (November 18, 1996)
  • K963132 — MINI STRIP/SERUM HCG (November 18, 1996)
  • K951705 — MINISTRIP HCG (October 3, 1995)

Other clearances for product code JJX

  • K170678 — Beta-CrossLaps CalCheck 5 (April 4, 2017)
  • K162173 — Elecsys CYFRA 21-1 CalCheck 5 (January 12, 2017)
  • K162514 — Multichem A1c (October 26, 2016)
  • K161874 — Audit MicroControls Linearity DROP LQ Blood Glucose (August 10, 2016)
  • K161526 — LIAISON CMV IgM Serum Control Set (June 30, 2016)
  • K161522 — LIAISON EBV IgM Serum Control Set (June 30, 2016)
  • K161082 — IDS-iSYS 17-OH Progesterone Control Set, IDS-iSYS 17-OH Progesterone Calibration (May 17, 2016)
  • K152117 — Dropper hsCRP High Sensitivity CRP Control (April 21, 2016)
  • K151742 — Contour Next Control Solution (September 23, 2015)
  • K143687 — ADVIA Centaur Follicle Stimulating Hormone (FSH) Master Curve Material, ADVIA Ce (July 17, 2015)

FDA data resources