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510(k) K760623

LANCER PARAPLAST HISTO PROCESS CASSETTE by Sherwood Medical Industries — Product Code IDZ

K760623 is an FDA 510(k) premarket notification submitted by Sherwood Medical Industries for the device "LANCER PARAPLAST HISTO PROCESS CASSETTE". The FDA issued a decision of Substantially Equivalent on September 27, 1976. The device falls under product code IDZ (Cassettes, Tissue), a Class I device regulated under 21 CFR 864.3010. Sherwood Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 1976
Date Received
September 13, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cassettes, Tissue
Device Class
Class I
Regulation Number
864.3010
Review Panel
PA
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 IDZ

  • K863483 — CASSETTE EMBOSSEER (September 16, 1986)
  • K862457 — LYNX EL MICROSCOPY TISSUE PROCESSOR (July 16, 1986)
  • K833857 — MACLEAN-FOGG, TISSUE CASSETTES (December 2, 1983)
  • K831334 — TISSUE CASSETTES FOR PROCESSING-EM BED (May 25, 1983)

FDA data resources