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

SPIROCARE 108-B

K Number: K782016 · Decision Dec 13, 1978
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
38
Review Days
8

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Basic Information

Device Name
SPIROCARE 108-B
K Number
K782016
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Marion Laboratories, Inc.
Date Received
December 5, 1978
Decision Date
December 13, 1978
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

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K874554 ENVICLUSIVE (TM)
K874551 ENVINET(TM)
K874552 ENVISAN PAD
K874553 ENVISAN PASTE
K870864 CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST
K863485 MODIFICATION OF CDT(TM) CLOSTRIDIUM TEST
K862123 BIOSPHERE ANAEROBIC ENVIRONMENTAL DEVICE
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