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510(k) K830482

ABUSCREEN RADIOIMMUNOASSAY-AMPHETAMINE by Hoffmann-La Roche, Inc. — Product Code DJP

K830482 is an FDA 510(k) premarket notification submitted by Hoffmann-La Roche, Inc. for the device "ABUSCREEN RADIOIMMUNOASSAY-AMPHETAMINE". The FDA issued a decision of Substantially Equivalent on March 24, 1983. The device falls under product code DJP (Radioimmunoassay, Amphetamine), a Class II device regulated under 21 CFR 862.3100. Hoffmann-La Roche, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 24, 1983
Date Received
February 15, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Amphetamine
Device Class
Class II
Regulation Number
862.3100
Review Panel
TX
Submission Type

Other clearances by Hoffmann-La Roche, Inc.

  • K850727 — BHCG-ROCHE EIA (June 25, 1985)
  • K831694 — RENAK (July 19, 1983)
  • K830460 — ABUSCREEN RADIOIMMUNOASSAY FOR MORPHINE (March 24, 1983)
  • K830481 — ABUSCREEN RADIOIMMUNOASSAY-PHENCYCLIDINE (March 24, 1983)
  • K830462 — ABUSCREEN RADIOUMMUNOASSAY--URINE (March 24, 1983)
  • K830461 — ABUSCREEN RADIOUMMUNOASSAY-METHAQUALONE (March 24, 1983)
  • K830480 — ABUSCREEN RADIOIMMUNOASSAY-COCAINE META (March 24, 1983)
  • K830479 — ABUSCREEN RADIOIMMUNOASSAY-BARBITURATE (March 10, 1983)
  • K823580 — COBAS REAGENT FOR INORGANIC PHOSPHORUS (January 7, 1983)
  • K823576 — COBAS STANDARD FOR TOTAL PROTEIN (January 7, 1983)

Other clearances for product code DJP

  • K960526 — PRIMIDONE EIA TEST (March 18, 1996)
  • K913866 — URINE AMPHETAMINE DIRECT RIA KIT (I-125) (September 25, 1991)
  • K912755 — ABUSCREEN RADIOIMMUNOASSAY FOR AMPHETAMINE (August 26, 1991)
  • K882228 — REVISED DOUBLE ANTIBODY AMPHETAMINE (August 8, 1988)
  • K881817 — ABUSCREEN(R) ONTRAK(TM) FOR AMPHETAMINES (July 29, 1988)
  • K854009 — ABUSCREEN RADIOIMMUNOASSAY FOR AMPHETAMINE-HIGH SP (October 15, 1985)
  • K823212 — ABUSCREEN RADIOIMMUNOASSAY - AMPHETAMINE (November 29, 1982)
  • K812986 — AGGLUTEX AMPHETAMINE TEST KIT (January 22, 1982)

FDA data resources