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

ROADRUNNER, PEP THERAPY DEVICE

K Number: K991561 · Decision Nov 10, 1999
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
8
Review Days
190

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Basic Information

Device Name
ROADRUNNER, PEP THERAPY DEVICE
K Number
K991561
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dhd Healthcare Corp.
Date Received
May 4, 1999
Decision Date
November 10, 1999
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)

Similar 510(k) Clearances

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Other Clearances by Dhd Healthcare Corp.

K Number Device Name
K040718 TRUST
K002768 ACAPELLA
K003146 CLINIFLO INCENTIVE SPIROMETER
K991300 BOEING, POSITIVE AIRWAY PRESSURE (PAP) THERAPY DEVICE
K983467 THERAPEP
K980662 LICHEN, BACTERIAL IN LINE BREATHING FILTER
K981167 STEALTH PILOT KIT/ STEALTH SPACER/FACE MASK KIT