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510(k) K891990

RUBEOLA IGG CLIN-ELISA TEST SYSTEM, CAT. #4600 by Clinical Sciences, Inc. — Product Code LJB

K891990 is an FDA 510(k) premarket notification submitted by Clinical Sciences, Inc. for the device "RUBEOLA IGG CLIN-ELISA TEST SYSTEM, CAT. #4600". The FDA issued a decision of Substantially Equivalent on June 15, 1989. The device falls under product code LJB (Enzyme Linked Immunoabsorbent Assay, Rubeola Igg), a Class I device regulated under 21 CFR 866.3520. Clinical Sciences, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 15, 1989
Date Received
March 28, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Rubeola Igg
Device Class
Class I
Regulation Number
866.3520
Review Panel
MI
Submission Type

The qualitative detection of measles specific IgG antibodies in serum or plasma.

Other clearances by Clinical Sciences, Inc.

  • K900688 — VARICELLA ZOSTER IGG CLIN-ELISA TEST KIT (May 15, 1990)
  • K883871 — EPSTEIN-BARR VIRAL CAPSID ANTIGEN IGM #5590 (July 14, 1989)
  • K883870 — EPSTEIN-BARR VIRAL CAPSID ANTIGEN IGG #4590 (July 14, 1989)
  • K883600 — EPSTEIN-BARR VIRUS (EBNA-1) IGG CATA. #4550 (May 11, 1989)
  • K883601 — EPSTEIN-BARR VIRUS (EBNA-1) IGM CATA. #5550 (May 11, 1989)
  • K874594 — TOXOPLASMA IGM CLIN-ELISA(TM) CAT # 5560 (March 7, 1988)
  • K872942 — IGM CMV CLIN-ELISA(TM) TEST SYSTEM NUMBER: 5530 (January 11, 1988)
  • K860145 — RUBELLA ELISA TEST SYSTEM CATALOG NUMBER: 4540 (July 14, 1986)
  • K860773 — TOXOPLASMA IGG CLIN-ELISA TEST KIT CAT. NO. 4560 (May 23, 1986)
  • K854666 — CYTOMEGALOVIRUS (CMV) ELISA TEST SYS. CAT. NO:4530 (February 5, 1986)

Other clearances for product code LJB

  • K974552 — DIAMEDIX IS-MEASLES IGG TEST SYSTEM (January 28, 1998)
  • K971620 — QUANTA LITE RUBEOLA (MEASLES) IGG (July 22, 1997)
  • K922335 — BARTELS RUBEOLA IGM EIA (September 2, 1992)
  • K922330 — BARTELS RUBEOLA IGG EIA (September 2, 1992)
  • K910290 — VIRATEST-DIA(TM) MEASLES (RUBEOLA) (March 18, 1992)
  • K904083 — RUBEOLA IGM ELISA TEST (January 3, 1991)
  • K903961 — MEASLES IGG MICROASSAY (December 28, 1990)
  • K904854 — RUBEOLA IGG ELISA TEST (December 4, 1990)
  • K873925 — VIRGO(TM) MEASLES IGG ELISA (February 24, 1988)
  • K821762 — MEASELISA TEST KIT (July 30, 1982)

FDA data resources