Medical Device Manufacturer · US , Mchenry , IL

Scripps-Miles, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1981

Total

Cleared

Denied

Scripps-Miles, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1981 to 1981. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Scripps-Miles, Inc. Filter by specialty or product code using the sidebar.

Scripps-Miles, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Scripps-Miles, Inc.

9 devices

1-9 of 9

Cleared Sep 23, 1981

SCRIPPSYSTEM IMMUNOGLOBIN RID KIT

K812453 · DEW

Immunology · 26d

Cleared Sep 08, 1981

SCRIPPSYSTEM NEPHELOMETRIC ANTISERA KIT

K812328 · DEW

Immunology · 21d

Cleared Jul 10, 1981

HEP-2-CRITHIDIA LUCILIAE ANA TEST KIT

K811714 · DHN

Immunology · 23d

Cleared Jun 16, 1981

SCRIPPSERA COMPLEMENT CONTROL SERA

K811433 · DHL

Immunology · 25d

Cleared Apr 08, 1981

SCRIPPSYSTEM C3 RID KIT

K810501 · CZW

Immunology · 43d

Cleared Apr 08, 1981

SCRIPPSYSTEM C4 RID KIT

K810502 · DBI

Immunology · 43d

Cleared Feb 09, 1981

SCRIPPSERA ANA REFERENCE CONTROL SERA

K810081 · DHN

Immunology · 27d

Cleared Feb 09, 1981

SCRIPPSYSTEM RHEUMATOID FACTOR LATEX KIT

K810141 · DHR

Immunology · 19d

Cleared Feb 09, 1981

SCRIPPSERA THEUMATOID FACTOR REFER. CNTL

K810221 · DHR

Immunology · 13d

Scripps-Miles, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Scripps-Miles, Inc.

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