FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DURALASTIC I AND DURALASTIC II

K Number: K971480 · Decision May 28, 1997
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
44
Applicant Total
9
Review Days
35

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Basic Information

Device Name
DURALASTIC I AND DURALASTIC II
K Number
K971480
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Allied Biomedical Corp.
Date Received
April 23, 1997
Decision Date
May 28, 1997
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
MIB Elastomer, Silicone Block

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MIB), ordered by most recent decision date.

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Other Clearances by Allied Biomedical Corp.

K Number Device Name
K982051 KELOCATE SHEETING
K971481 DURALASTIC ANATOMICAL NASAL IMPLANTS
K971479 DURALASTIC ANATOMICAL MALAR IMPLANTS
K971478 DURALASTIC ANATOMICAL CHIN IMPLANTS
K955368 DURALASTIC I
K955370 DURALASTIC II
K955433 DURALASTIC SILICONE TUBING
K954413 KELOCOTE