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

CONTAINER SYSTEM

K Number: K792558 · Decision Dec 27, 1979
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
13
Review Days
15

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Basic Information

Device Name
CONTAINER SYSTEM
K Number
K792558
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Aesculap Instruments Corp.
Date Received
December 12, 1979
Decision Date
December 27, 1979
Product Code
FLE
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
FLE Sterilizer, Steam

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Other Clearances by Aesculap Instruments Corp.

K Number Device Name
K885046 INSITUCAT VALVE STRIPPER
K890182 PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV
K890443 CASPAR SCALP CLIP, APPLIER
K893121 ROBOTRAC (TM) RETRACTOR ARM
K884057 ELAN-E DISPOSABLE DRAPE
K880704 CERULLO SUCTION REGULATOR
K860016 AESCULAP BONE MILL
K801888 HANDPIECE, DENTAL
K801886 BURR, DENTAL
K801887 DRILL, DENTAL
Search all 13 clearances from Aesculap Instruments Corp. →