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510(k) K760621

LANCER PLASTIC TRANSFER PIPETTE by Sherwood Medical Industries — Product Code JRC

K760621 is an FDA 510(k) premarket notification submitted by Sherwood Medical Industries for the device "LANCER PLASTIC TRANSFER PIPETTE". The FDA issued a decision of Substantially Equivalent on October 5, 1976. The device falls under product code JRC (Micro Pipette), a Class I device regulated under 21 CFR 862.2050. Sherwood Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 1976
Date Received
September 13, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Micro Pipette
Device Class
Class I
Regulation Number
862.2050
Review Panel
CH
Submission Type

Other clearances by Sherwood Medical Industries

  • K801070 — SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES (July 21, 1980)
  • K801071 — LANCER GLUCOSE RATE REAGENT KIT (May 23, 1980)
  • K792013 — LANCER L-INA HUMAN REFERENCE SERUM (November 13, 1979)
  • K792014 — LANCER L-INA BUFFER, POLYMER, WASH SOLU (November 13, 1979)
  • K782077 — LANCER ICE CUBE (April 3, 1979)
  • K790523 — ARGYLE ESOPHAGEAL STETHOSCOPE (March 27, 1979)
  • K790196 — MONOJECT ARTERIAL BLOOD SAMPLING DEVICE (March 13, 1979)
  • K790197 — REAGENT KIT, LANCER GLUCOSE (March 12, 1979)
  • K781459 — MONOJECT SCALE MAGNIFIER (October 24, 1978)
  • K781060 — MONOJECT ENDOSSEOUS DENTAL IMPLANT (August 14, 1978)

Other clearances for product code JRC

  • K840186 — SMI DIGITRON (April 5, 1984)
  • K834100 — PRE-CALIBRATED PIPETTES (February 21, 1984)
  • K822078 — DADE DISP. DISPENSING-SPREADING PIPETS (July 27, 1982)
  • K792696 — MICROPITETTE (February 1, 1980)
  • K770594 — LABORATORY EXPENDABLE PRODUCTS (July 6, 1977)

FDA data resources