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510(k) K912242

PROSPECT(TM/CRYPTOSPORIDIUM by Alexon, Inc. — Product Code MHJ

K912242 is an FDA 510(k) premarket notification submitted by Alexon, Inc. for the device "PROSPECT(TM/CRYPTOSPORIDIUM". The FDA issued a decision of Substantially Equivalent on March 23, 1992. The device falls under product code MHJ (Cryptosporidium Spp.), a Class II device regulated under 21 CFR 866.3220. Alexon, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 1992
Date Received
May 21, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cryptosporidium Spp.
Device Class
Class II
Regulation Number
866.3220
Review Panel
MI
Submission Type

Other clearances by Alexon, Inc.

  • K934493 — PROSPECT MICROPLATE ASSAY (September 20, 1994)
  • K942098 — PROSPECT GIARDIA (September 9, 1994)
  • K931147 — PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATION (May 13, 1993)
  • K930451 — PROSPEC T GIARDIA MICROTITER ASSAY (April 21, 1993)
  • K922675 — PROSPECT GIARDIA CONTROLS (September 11, 1992)
  • K922010 — PROSPECT(TM) GIARDIA MICROTITER ASSAY/MODIFICATION (June 19, 1992)
  • K920817 — MODIFICATION PROSPECT GIARDIA RAPID ASSAY (April 22, 1992)
  • K915093 — PROSPECT(TM) GIARDIA RAPID ASSAY (January 30, 1992)
  • K911337 — PROSPEC T/GIARDIA RAPID ASSAY (September 27, 1991)

Other clearances for product code MHJ

  • K171078 — TRI-COMBO PARASITE SCREEN (July 10, 2017)
  • K121565 — UNI-GOLD CRYPTOSPORIDIUM (February 8, 2013)
  • K051929 — GIARDIA/CRYPTOSPORIDIUM CHEK (November 17, 2005)
  • K052932 — CRYPTOSPORIDIUM II (November 4, 2005)
  • K031965 — XPECT CRYPTOSPORIDIUM LATERAL FLOW ASSAY, MODEL 2451020 (November 14, 2003)
  • K031059 — IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96 (July 10, 2003)
  • K982764 — PREMIER CRYPTOSPORIDIUM (December 3, 1998)
  • K982709 — MODIFICATION TO PROSPECT CRYPTOSPORIDIUM MICROTITER ASSAY (September 3, 1998)
  • K980354 — CRYPTOSPORIDIUM TEST (May 18, 1998)
  • K955852 — CRYPTO-CEL IF TEST (August 5, 1996)

FDA data resources