FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
P-AMYLASE CONTROL
K Number: K935362
·
Decision Jan 27, 1994
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
6
Review Days
84
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Basic Information
- Device Name
- P-AMYLASE CONTROL
- K Number
- K935362
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Beckman
- Date Received
- November 4, 1993
- Decision Date
- January 27, 1994
- Product Code
- JJX
- 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 |
|---|---|---|---|
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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| K Number | Device Name | ||
|---|---|---|---|
| K991707 | MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206 | Jun 1, 1999 | Substantially Equivalent |
| K971534 | SYNCHRON SYUSTEMS DAT DRUG FREE URINE CONTROL | May 21, 1997 | Substantially Equivalent |
| K904219 | SYNCHRON CX 7 CLINICAL ANALYZER | Oct 22, 1990 | Substantially Equivalent |
| K904220 | SYNCHRON CX4-CE | Oct 15, 1990 | Substantially Equivalent |
| K893583 | BECKMAN CHOLINESTERASE REAGENT KIT | Aug 15, 1989 | Substantially Equivalent |