FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DISPOSABLE MULTIPLE LIGATING CLIP
K Number: K820837
·
Decision May 28, 1982
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
13
Applicant Total
204
Review Days
63
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Basic Information
- Device Name
- DISPOSABLE MULTIPLE LIGATING CLIP
- K Number
- K820837
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- ETHICON, Inc.
- Date Received
- March 26, 1982
- Decision Date
- May 28, 1982
- Product Code
- GDO
- 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 |
|---|---|---|---|
| GDO | Applier, Surgical, Clip | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GDO), ordered by most recent decision date.
UNICLIP SURGICAL CLIP APPLIER
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MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APP
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TOWEL CLIPS
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SUTURE CLIP APPLIER/REMOVER
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ETHICON MULTIPLE LIGATING CLIP APPLIER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
HEMOSPENSER CARTRIDGE CAT. NO. 523500-
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
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