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

ATTACHABLE LANZ (TENTATIVE)

K Number: K885216 · Decision Mar 14, 1989
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
38
Applicant Total
7
Review Days
85

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Basic Information

Device Name
ATTACHABLE LANZ (TENTATIVE)
K Number
K885216
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5750
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Mallinckroot, Inc.
Date Received
December 19, 1988
Decision Date
March 14, 1989
Product Code
BSK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSK Cuff, Tracheal Tube, Inflatable

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K Number Device Name
K983830 COPPERHEAD 5 FR. PTA CATHETER, FINCH 4 FR. PTA CATHETER
K894445 MODIFIED SOFTOUCH INTRODUCER W/HEMO VALVE & SIDE
K885348 A-V(TM) SOFTOUCH UHF CARDIAC PIGTAIL
K884159 SOFTOUCH INTRODUCER W/HEMOSTASIS VALVE & SIDEPORT
K884481 CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE
K882130 FOLEY-TEMP(TM)