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

RUSCH MANUAL RESUSCITATOR BAG

K Number: K993194 · Decision Mar 24, 2000
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
26
Review Days
183

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Basic Information

Device Name
RUSCH MANUAL RESUSCITATOR BAG
K Number
K993194
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rusch, Inc.
Date Received
September 23, 1999
Decision Date
March 24, 2000
Product Code
BTM
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
BTM Ventilator, Emergency, Manual (Resuscitator)

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Other Clearances by Rusch, Inc.

K Number Device Name
K010420 RUSCH MMG/O'NEIL CATHETER
K993528 RUSCH EMERGENCY MASK
K980870 RUSCH SILICONE FOLEY CATHETER
K974419 RUSCH SIMPLASTIC COUNCILL TIP CATHETER
K963779 RUSCH ENTERAL FEEDING TUBE
K970021 RUSCH SUPRAPUBIC TRAY
K963993 RUSCH SIMPLASTIC FOLEY CATHETERIZATION SET
K955564 RUSCH ULTRA TRACHEOFLEX TRACHEOSTOMY SET, CUFFED, STERILE
K955495 RUSCH REINFORCED TRACHAEL TUBE CUFFED, STERILE
K953963 RUSCH SINGLE LUMEN BRONCHIAL TUVBE SET, STERILE, FOR LEFT & RIGHT SIDED BRONCHIAL INTUBATION
Search all 26 clearances from Rusch, Inc. →