FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DURALASTIC I
K Number: K955368
·
Decision Feb 8, 1996
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
44
Applicant Total
9
Review Days
78
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Basic Information
- Device Name
- DURALASTIC I
- K Number
- K955368
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.3620
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Allied Biomedical Corp.
- Date Received
- November 22, 1995
- Decision Date
- February 8, 1996
- Product Code
- MIB
- Advisory Committee
- Ear, Nose, Throat
- 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 |
|---|---|---|---|
| MIB | Elastomer, Silicone Block | FDA class 2 | Ear, Nose, Throat |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (MIB), ordered by most recent decision date.
MISTI Silicone Implant
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ShiNeo Silicone Implant
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AugMENTA Penile Implant
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FDA Class 2
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FDA Class 2
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BioSiCar Silicone Implant
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Other Clearances by Allied Biomedical Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K982051 | KELOCATE SHEETING | Aug 5, 1998 | Substantially Equivalent |
| K971481 | DURALASTIC ANATOMICAL NASAL IMPLANTS | Jul 18, 1997 | Substantially Equivalent |
| K971479 | DURALASTIC ANATOMICAL MALAR IMPLANTS | Jul 18, 1997 | Substantially Equivalent |
| K971478 | DURALASTIC ANATOMICAL CHIN IMPLANTS | Jul 18, 1997 | Substantially Equivalent |
| K971480 | DURALASTIC I AND DURALASTIC II | May 28, 1997 | Substantially Equivalent |
| K955370 | DURALASTIC II | Feb 8, 1996 | Substantially Equivalent |
| K955433 | DURALASTIC SILICONE TUBING | Jan 26, 1996 | Substantially Equivalent |
| K954413 | KELOCOTE | Nov 29, 1995 | Substantially Equivalent |