FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFIED TSH IRMA KIT
K Number: K883742
·
Decision Jan 3, 1989
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
29
Review Days
124
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Basic Information
- Device Name
- MODIFIED TSH IRMA KIT
- K Number
- K883742
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1690
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Pacific Biotech, Inc.
- Date Received
- September 1, 1988
- Decision Date
- January 3, 1989
- Product Code
- JLW
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JLW | Radioimmunoassay, Thyroid-Stimulating Hormone | FDA class 2 | Clinical Chemistry |
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Other Clearances by Pacific Biotech, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K924461 | STREP A NEGATIVE CONTROL | Dec 2, 1993 | Substantially Equivalent |
| K902510 | CARDS O.S. MONO | Jul 16, 1990 | Substantially Equivalent |
| K896482 | PERFECT(TM) ONE STEP EARLY PREGNANCY TEST KIT | Mar 6, 1990 | Substantially Equivalent |
| K896221 | CARDS O.S.(TM) STREP A | Dec 13, 1989 | Substantially Equivalent |
| K895390 | CARDS O.S. (TM) HCG-URINE | Nov 13, 1989 | Substantially Equivalent |
| K891770 | HCG IRMA II | May 24, 1989 | Substantially Equivalent |
| K884616 | FIRSTDAY EARLY PREGNANCY TESTING KIT II | Jan 13, 1989 | Substantially Equivalent |
| K884007 | CARDS(TM) MONO | Nov 18, 1988 | Substantially Equivalent |
| K882895 | MODIFIED BETA QUIK STAT EIA KIT | Oct 12, 1988 | Substantially Equivalent |
| K883639 | MODIFIED HCG IRMA KIT | Oct 6, 1988 | Substantially Equivalent |