FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SAPH-LOOP LIGATING LOOP
K Number: K022410
·
Decision Aug 20, 2002
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
4
Review Days
27
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Basic Information
- Device Name
- SAPH-LOOP LIGATING LOOP
- K Number
- K022410
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 878.5000
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Genzyme Biosurgery
- Date Received
- July 24, 2002
- Decision Date
- August 20, 2002
- Product Code
- GAT
- 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 |
|---|---|---|---|
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Genzyme Biosurgery
| K Number | Device Name | ||
|---|---|---|---|
| K031554 | S-1150 PLEUR-EVAC SAHARA PLUS CONTINUOUS REINFUSION AUTOTRANSFUSION SYSTEM | Jul 25, 2003 | Substantially Equivalent |
| K030212 | MONODEK SYNTHETIC ABSORBABLE SURGICAL SUTURE | Mar 27, 2003 | Substantially Equivalent |
| K022989 | RADLITE TISSUE RETRACTOR SYSTEM | Nov 25, 2002 | Substantially Equivalent |