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

EXERCISER, RESP., DEEP BREATHING

K Number: K780037 · Decision Feb 24, 1978
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
12
Review Days
46

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Basic Information

Device Name
EXERCISER, RESP., DEEP BREATHING
K Number
K780037
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Medical Technologies of Georgia
Date Received
January 9, 1978
Decision Date
February 24, 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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Other Clearances by Medical Technologies of Georgia

K Number Device Name
K973120 READYCATH CATHETER
K952392 MLI SET
K911129 MMG BILE BAG
K873136 MMG CATH-N-PLACE
K871949 MMG DELEE SUCTION CATHETER W/MUCOUS TRAP
K854821 MMG EXTERNAL FEMALE CATHETERS
K854660 THE MMG ENTERAL FEEDING ADMINISTRATION SET
K840839 MMG FOLEY CATHETER
K840897 OXYGEN TUBING
K821854 U-200 BAG
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