FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PHADEBAS ISOAMYLASE TEST
K Number: K810584
·
Decision May 13, 1981
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
7
Applicant Total
129
Review Days
70
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Basic Information
- Device Name
- PHADEBAS ISOAMYLASE TEST
- K Number
- K810584
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1070
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Pharmacia, Inc.
- Date Received
- March 4, 1981
- Decision Date
- May 13, 1981
- Product Code
- CIW
- 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 |
|---|---|---|---|
| CIW | Starch-Dye Bound Polymer, Amylase | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
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ENZYMATIC ALPHA-AMYLASE REAGENT KIT
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PANTRAK E.K.
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Other Clearances by Pharmacia, Inc.
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|---|---|---|---|
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| K970420 | MASTERCAP AM 5.0/MASTERCAP RM 5.0 | Jun 30, 1997 | Substantially Equivalent |
| K964152 | UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH | Apr 23, 1997 | Substantially Equivalent |
| K962274 | UNICAP 100 | Sep 12, 1996 | Substantially Equivalent |
| K941993 | PHARMACIA CAP SYSTEM PHADIATOP FEIA | Jan 30, 1996 | Substantially Equivalent |
| K954337 | GENOTROPIN MIXER | Nov 13, 1995 | Substantially Equivalent |
| K951025 | PISTON SYRINGE | Oct 19, 1995 | Substantially Equivalent |
| K952025 | ROBOCAP | Jul 26, 1995 | Substantially Equivalent |