FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
UNIVERSAL TOURNIQUET
K Number: K873928
·
Decision Oct 23, 1987
Classifications
1
FEI Numbers
335
Registration Numbers
335
Same Product Code
19
Applicant Total
21
Review Days
28
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Basic Information
- Device Name
- UNIVERSAL TOURNIQUET
- K Number
- K873928
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.5900
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Dryden Corp.
- Date Received
- September 25, 1987
- Decision Date
- October 23, 1987
- Product Code
- GAX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| GAX | Tourniquet, Nonpneumatic | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
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DALE VENIPUNCTURE TOURNIQUET, PRODUCT NO. 1335
FDA 510(k)
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Other Clearances by Dryden Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K880923 | PATIENT VENTILATOR ISOLATOR | Sep 6, 1988 | Substantially Equivalent |
| K880769 | BREATHING CIRCUIT W/HEATED WIRE | Aug 24, 1988 | Substantially Equivalent |
| K882285 | NONREBREATHING CIRCUIT | Aug 16, 1988 | Substantially Equivalent |
| K873927 | REUSEABLE BREATHING TUBES | Oct 20, 1987 | Substantially Equivalent |
| K870859 | BAG-TAIL BLEED VALVE | Aug 3, 1987 | Substantially Equivalent |
| K871386 | BREATHING CIRCUIT | May 29, 1987 | Substantially Equivalent |
| K870858 | BADGWELL SAMPLING CATHETER | May 14, 1987 | Substantially Equivalent |
| K861540 | DISPOSABLE BERMAN AND GUEDEL AIRWAYS | May 2, 1986 | Substantially Equivalent |
| K850644 | NASOPHARYNGEAL AIRWAY-ROBERTAZZI | Mar 21, 1985 | Substantially Equivalent |
| K842843 | DRYDEN SCAVENGER INTERFACE SYSTEM | Jul 27, 1984 | Substantially Equivalent |