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

NONREBREATHING CIRCUIT

K Number: K882285 · Decision Aug 16, 1988
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
21
Review Days
76

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Basic Information

Device Name
NONREBREATHING CIRCUIT
K Number
K882285
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Dryden Corp.
Date Received
June 1, 1988
Decision Date
August 16, 1988
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BTM), ordered by most recent decision date.

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Other Clearances by Dryden Corp.

K Number Device Name
K880923 PATIENT VENTILATOR ISOLATOR
K880769 BREATHING CIRCUIT W/HEATED WIRE
K873928 UNIVERSAL TOURNIQUET
K873927 REUSEABLE BREATHING TUBES
K870859 BAG-TAIL BLEED VALVE
K871386 BREATHING CIRCUIT
K870858 BADGWELL SAMPLING CATHETER
K861540 DISPOSABLE BERMAN AND GUEDEL AIRWAYS
K850644 NASOPHARYNGEAL AIRWAY-ROBERTAZZI
K842843 DRYDEN SCAVENGER INTERFACE SYSTEM
Search all 21 clearances from Dryden Corp. →