FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DESERET CATHETER DRESSING
K Number: K812073
·
Decision Oct 6, 1981
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
50
Review Days
77
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Basic Information
- Device Name
- DESERET CATHETER DRESSING
- K Number
- K812073
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5240
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Warner-Lambert Co.
- Date Received
- July 21, 1981
- Decision Date
- October 6, 1981
- Product Code
- KGX
- Advisory Committee
- General Hospital
- 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 |
|---|---|---|---|
| KGX | Tape And Bandage, Adhesive | FDA class 1 | General Hospital |
Similar 510(k) Clearances
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TARGETT PATCH
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PARALLEL
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|---|---|---|---|
| K024160 | NEOSPORIN SCAR SOLUTION | Mar 17, 2003 | Substantially Equivalent |
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| K870584 | O.P.T.(TM) OVULATION PREDICTION TEST | Nov 25, 1987 | Substantially Equivalent |
| K861510 | MULTILUMEN VIAPIC CENTRAL LINE CATHETER | Jun 9, 1986 | Substantially Equivalent |
| K852689 | GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK | Aug 19, 1985 | Substantially Equivalent |
| K852967 | GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISK | Aug 19, 1985 | Substantially Equivalent |
| K852843 | GENERAL DIAGNOSTICS COAG-A-MATE XC | Aug 13, 1985 | Substantially Equivalent |
| K852889 | GENERAL DIAGNOSTICS RAPID E. COLI TEST | Jul 23, 1985 | Substantially Equivalent |
| K850409 | GEN. DIAG. CHROMOSTRATE REF. PLASMA | May 8, 1985 | Substantially Equivalent |
| K850412 | GEN. DIAG. CHROMOSTRATE ANTITHROMBIN III ASSAY | May 8, 1985 | Substantially Equivalent |