FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
OLYMPUS AU 5000 FLAME PHOTOMETER MODULE
K Number: K862148
·
Decision Sep 29, 1986
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
21
Applicant Total
142
Review Days
117
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Basic Information
- Device Name
- OLYMPUS AU 5000 FLAME PHOTOMETER MODULE
- K Number
- K862148
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2540
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Olympus Corp.
- Date Received
- June 4, 1986
- Decision Date
- September 29, 1986
- Product Code
- JJO
- 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 |
|---|---|---|---|
| JJO | Flame Emission Photometer For Clinical Use | FDA class 1 | Clinical Chemistry |
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Other Clearances by Olympus Corp.
| K Number | Device Name | ||
|---|---|---|---|
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| K942338 | OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES | Nov 30, 1994 | Substantially Equivalent |
| K931763 | HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS | Aug 29, 1994 | Substantially Equivalent |
| K934835 | FLOVAL | Jun 21, 1994 | Substantially Equivalent |
| K931764 | HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES | Jun 8, 1994 | Substantially Equivalent |
| K915857 | FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE | Mar 11, 1994 | Substantially Equivalent |
| K931994 | RESECTOSCOPE SHEATH | Feb 17, 1994 | Substantially Equivalent |
| K933992 | OLYMPUS SCLEROTHERAPY BALLOON | Dec 21, 1993 | Substantially Equivalent |
| K934361 | OLYMPUS CREATININE REAGENT | Nov 16, 1993 | Substantially Equivalent |