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

THREE PORT SENSOR MANIFOLD

K Number: K841637 · Decision May 2, 1984
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
87
Applicant Total
21
Review Days
12

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Basic Information

Device Name
THREE PORT SENSOR MANIFOLD
K Number
K841637
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5975
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Dryden Corp.
Date Received
April 20, 1984
Decision Date
May 2, 1984
Product Code
BZO
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
BZO Set, Tubing And Support, Ventilator (W Harness)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BZO), 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
K882285 NONREBREATHING CIRCUIT
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
Search all 21 clearances from Dryden Corp. →