FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CURVED HEMOSTAT 5

K Number: K831138 · Decision May 18, 1983
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
72
Applicant Total
21
Review Days
41

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Basic Information

Device Name
CURVED HEMOSTAT 5
K Number
K831138
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Almore Intl., Inc.
Date Received
April 7, 1983
Decision Date
May 18, 1983
Product Code
HTD
Advisory Committee
General, Plastic Surgery
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
HTD Forceps

Similar 510(k) Clearances

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Other Clearances by Almore Intl., Inc.

K Number Device Name
K862851 ALMORE FACE MASK
K854692 MONARCH II BLEACHING INSTRUMENT
K854696 OP II VISIBLE LIGHT CURING SYSTEM
K854690 DIAMONDS BURS-COMPOSIT FINISHING
K854691 DIAMOND BURS-HANDPIECE
K854700 EZ-ON TUBING CONDITIONER (LUBRICANT)
K854702 PLASTIC MOUNTING RINGS
K854701 RETRACT-A-CORD
K854697 TUBING HANDPIECE REPLACEMENT
K854699 TUBING SYRING
Search all 21 clearances from Almore Intl., Inc. →