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510(k) K852480

DERM-KIT by Culture Kits, Inc. — Product Code JSI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 9, 1985
Date Received
June 11, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, Selective And Differential
Device Class
Class I
Regulation Number
866.2360
Review Panel
MI
Submission Type

Other clearances by Culture Kits, Inc.

  • K911846 — URI-THREE(TM), MODIFICATION (October 4, 1991)
  • K854672 — CANDI-KIT TM (July 11, 1986)
  • K853488 — STAPH KIT (August 28, 1985)
  • K851225 — URINE DUO (August 13, 1985)
  • K852582 — GONI-KIT (July 12, 1985)
  • K851518 — MUELLER HINTON SENSITIVITY PLATE (April 29, 1985)
  • K850765 — STREP-KIT (April 24, 1985)
  • K850998 — URI-KIT (April 1, 1985)

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  • K881572 — XL AGAR BASE (April 18, 1988)
  • K881577 — MODIFIED SELECTIVE STREPTOCOCCUS AGAR (April 18, 1988)
  • K881576 — SELENITE BROTH (April 18, 1988)
  • K881555 — TINSDALE AGAR BASE (April 18, 1988)
  • K881556 — TRICHOMONAS BROTH (April 18, 1988)