FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BASIN PACK
K Number: K802538
·
Decision Oct 31, 1980
Classifications
1
FEI Numbers
221
Registration Numbers
221
Same Product Code
8
Applicant Total
30
Review Days
16
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Basic Information
- Device Name
- BASIN PACK
- K Number
- K802538
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6730
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Texas Medical Products, Inc.
- Date Received
- October 15, 1980
- Decision Date
- October 31, 1980
- Product Code
- FNY
- Advisory Committee
- General Hospital
- 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 |
|---|---|---|---|
| FNY | Basin, Emesis | FDA class 1 | General Hospital |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (FNY), ordered by most recent decision date.
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Other Clearances by Texas Medical Products, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K893417 | SURGIFRESH SUB-MICRON MASK NO. 901008-000 | Jun 22, 1989 | Substantially Equivalent |
| K870932 | SURGIFRESH SURGICAL SMOKE REMOVAL | Mar 31, 1987 | Substantially Equivalent |
| K851575 | DR. BRUNO LNAGE MINI PHOTOMETER | Oct 18, 1985 | Substantially Equivalent |
| K830634 | CARDIOTOMY FILTER | Jun 30, 1983 | Substantially Equivalent |
| K813587 | DISPOSABLE THORACIC CATHETER | Jan 12, 1982 | Substantially Equivalent |
| K810532 | DISPOSABLE STOPCOCK | Apr 23, 1981 | Substantially Equivalent |
| K810515 | DISPOSABLE 2-STAGE CANNULA | Apr 23, 1981 | Substantially Equivalent |
| K810395 | PRE-BYPASS FILTER | Mar 5, 1981 | Substantially Equivalent |
| K802545 | CARDIOPLEGIC SETS | Jan 16, 1981 | Substantially Equivalent |
| K802543 | RIDGID VENA CAVA CANNULAE | Jan 16, 1981 | Substantially Equivalent |