FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CASTLE PROCEDURE AND RITTER EXAM. TABLES
K Number: K810900
·
Decision Apr 21, 1981
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
13
Applicant Total
37
Review Days
18
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Basic Information
- Device Name
- CASTLE PROCEDURE AND RITTER EXAM. TABLES
- K Number
- K810900
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4960
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Sybron Corp.
- Date Received
- April 3, 1981
- Decision Date
- April 21, 1981
- Product Code
- LGX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| LGX | Table, Examination, Medical, Powered | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LGX), ordered by most recent decision date.
ECHOCARDIOGRAPHY
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Other Clearances by Sybron Corp.
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|---|---|---|---|
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| K844092 | DIAGNOSTIC MICROSOPCE SLIDES | Oct 25, 1984 | Substantially Equivalent |
| K842132 | TYCOS SELF-CHECK/DIGITAL FEVER THERMO | Jul 18, 1984 | Substantially Equivalent |
| K841910 | KERR SEALAPEX ROOT CANAL SEALER | Jul 13, 1984 | Substantially Equivalent |
| K841732 | LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM | Jun 5, 1984 | Substantially Equivalent |
| K840469 | TYCOS SELF CHECK BPM3 BLOOD PRESS MONI | May 21, 1984 | Substantially Equivalent |
| K840407 | KERR RESIN BONDED BRIDGE CEMENT | May 21, 1984 | Substantially Equivalent |
| K840607 | LF MOTORIZED RADIOGRAPHIC FILM VIEWER | Mar 5, 1984 | Substantially Equivalent |
| K833138 | DIGITAL INJECTOR SYS | Nov 14, 1983 | Substantially Equivalent |