FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇳 China

AM GLOVES STERILE VINYL EXAMINATION

K Number: K910774 · Decision Mar 7, 1991
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
2
Review Days
13

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Basic Information

Device Name
AM GLOVES STERILE VINYL EXAMINATION
K Number
K910774
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Am Gloves Co., Ltd.
Date Received
February 22, 1991
Decision Date
March 7, 1991
Product Code
LYZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYZ Vinyl Patient Examination Glove

Similar 510(k) Clearances

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

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Other Clearances by Am Gloves Co., Ltd.

K Number Device Name
K890985 VINYL PATIENT EXAMINATION GLOVE