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510(k) K872910

IMMUNO/SLE by Immunostics Co., Inc. — Product Code DHC

K872910 is an FDA 510(k) premarket notification submitted by Immunostics Co., Inc. for the device "IMMUNO/SLE". The FDA issued a decision of Substantially Equivalent on August 12, 1987. The device falls under product code DHC (System, Test, Systemic Lupus Erythematosus), a Class II device regulated under 21 CFR 866.5820. Immunostics Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 1987
Date Received
July 24, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Systemic Lupus Erythematosus
Device Class
Class II
Regulation Number
866.5820
Review Panel
IM
Submission Type

Other clearances by Immunostics Co., Inc.

  • K926569 — IMMUNO RA UNDILUTED (April 6, 1993)
  • K902360 — HEMA-SCREEN (July 27, 1990)
  • K894780 — IMMUNO/ASO (October 16, 1989)
  • K883685 — IMMUNO/FEBRILE ANTIGENS (September 28, 1988)
  • K863741 — IMMUNO-CEPT D (BETA-MONOCLONAL) (November 13, 1986)
  • K854619 — DETECTACULT (March 3, 1986)
  • K853105 — IMMUNO-IM (September 3, 1985)
  • K842110 — SLIDE PREGNANCY TEST (July 12, 1984)
  • K834391 — IMMUNO-RA (February 3, 1984)
  • K834390 — IMMUNO-CRP (February 3, 1984)

Other clearances for product code DHC

  • K001352 — REAADS IGG ANTI-PROTHROMBIN SEMI-QUANTITATIVE TEST KIT (April 9, 2001)
  • K001398 — REAADS IGM ANTI-PROTHROMBIN SEMI-QUANTITATIVE TEST KIT (March 30, 2001)
  • K930247 — HUMAN A-DS DNA EIA KIT FOR DIAGNOSTIC USE (March 10, 1993)
  • K930421 — ELIAS DSDNA ABS (March 10, 1993)
  • K914801 — IMMUNOWELL DSDNA ANTIBODY TEST (December 9, 1991)
  • K885048 — ACCESS R-CLONE ANA PROFILE ASSAY (January 24, 1989)
  • K821385 — SERO/TEX LE TEST (May 28, 1982)
  • K810981 — ANTI NDNA IMMUNOFLOURESCENT TEST SYS (April 29, 1981)
  • K810226 — SLE ANTI-N-DNA LATEX TEST (February 9, 1981)
  • K800991 — CORDIA N (May 8, 1980)

FDA data resources