FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇳 India

PROBE SURGEON'S GLOVES- STERILE

K Number: K905624 · Decision Apr 8, 1991
Classifications
1
FEI Numbers
138
Registration Numbers
138
Same Product Code
558
Applicant Total
2
Review Days
115

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Basic Information

Device Name
PROBE SURGEON'S GLOVES- STERILE
K Number
K905624
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4460
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Glove India Pvt. , Ltd.
Date Received
December 14, 1990
Decision Date
April 8, 1991
Product Code
KGO
Advisory Committee
General, Plastic Surgery
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
KGO Surgeon'S Gloves

Similar 510(k) Clearances

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

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Other Clearances by Glove India Pvt. , Ltd.

K Number Device Name
K897187 PROBE PATIENT EXAMINATION GLOVES