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510(k) K760789

PH METER-130 (.001 PH) by Corning Medical & Scientific — Product Code JQY

K760789 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "PH METER-130 (.001 PH)". The FDA issued a decision of Substantially Equivalent on November 16, 1976. The device falls under product code JQY (Ph Meter), a Class I device regulated under 21 CFR 862.2050. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 1976
Date Received
September 10, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ph Meter
Device Class
Class I
Regulation Number
862.2050
Review Panel
CH
Submission Type

Other clearances by Corning Medical & Scientific

  • K875122 — DISPOSABLE STERILE SYRINGE FILTERS (January 12, 1988)
  • K872273 — CORNING EASY WASH ELISA PLATES (July 7, 1987)
  • K872076 — CORNING DISPOSABLE ROLLER BOTTLES (June 15, 1987)
  • K863789 — CORNING ELISA PLATES (October 3, 1986)
  • K854024 — CORNING MAGIC MAB HCG RADIOIMMUNOASSAY (November 26, 1985)
  • K853634 — CORNING CELL WELLS-MULTIPLE WELL PLATES (September 16, 1985)
  • K851939 — CORNING CERTAIN -ISE (June 14, 1985)
  • K851329 — MAGIC MONOCLONAL ANTIBODY TSH(MAB TSH)RADIOIMMUNOA (June 13, 1985)
  • K850806 — CORNING BLOOD COLLECTION CAPILLARY TUBES (March 25, 1985)
  • K850617 — CORNING 780 FLUOROMETER/DENSITOMETER (March 12, 1985)

Other clearances for product code JQY

  • K952178 — PH-DETECT TEST (October 20, 1995)
  • K905146 — OLYMPUS URINE PH (February 4, 1991)
  • K872888 — CIBA CORNING 288 PH/BLOOD GAS SYSTEM (August 25, 1987)
  • K770347 — METER, PH, DIGITAL, MODEL 3560 (April 15, 1977)
  • K770352 — METER, IV PH, MODEL EXPANDOMATIC (April 8, 1977)
  • K770351 — METER, IV PH, MODEL ZEROMATIC (April 5, 1977)
  • K760788 — PH METER-125 (.01 PH) (November 16, 1976)

FDA data resources