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

LINEN (HUCK) TOWEL

K Number: K862577 · Decision Jul 23, 1986
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
3
Review Days
16

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Basic Information

Device Name
LINEN (HUCK) TOWEL
K Number
K862577
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dimed, Intl.
Date Received
July 7, 1986
Decision Date
July 23, 1986
Product Code
KKX
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
KKX Drape, Surgical, Antimicrobial

Similar 510(k) Clearances

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

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Other Clearances by Dimed, Intl.

K Number Device Name
K870373 STERILE PROCEDURAL TRAYS
K864454 THERMOSTABLE NUCLEASE TEST AGAR