FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BREATHING CIRCUIT

K Number: K871386 · Decision May 29, 1987
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
21
Review Days
52

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BREATHING CIRCUIT
K Number
K871386
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5240
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Dryden Corp.
Date Received
April 7, 1987
Decision Date
May 29, 1987
Product Code
CAI
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
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)

Similar 510(k) Clearances

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

View all

Other Clearances by Dryden Corp.

K Number Device Name
K880923 PATIENT VENTILATOR ISOLATOR
K880769 BREATHING CIRCUIT W/HEATED WIRE
K882285 NONREBREATHING CIRCUIT
K873928 UNIVERSAL TOURNIQUET
K873927 REUSEABLE BREATHING TUBES
K870859 BAG-TAIL BLEED VALVE
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. →