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

H-H HARRIS NEONATAL NASAL CANNULA SET FOR CPAP

K Number: K871351 · Decision May 14, 1987
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
42
Review Days
38

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
H-H HARRIS NEONATAL NASAL CANNULA SET FOR CPAP
K Number
K871351
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Holter-Hausner Intl.
Date Received
April 6, 1987
Decision Date
May 14, 1987
Product Code
BZD
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
BZD Ventilator, Non-Continuous (Respirator)

Similar 510(k) Clearances

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

View all

Other Clearances by Holter-Hausner Intl.

K Number Device Name
K875287 H-H FLUSHING RESERVOIR
K874508 H-H EXTERNAL VENTRICULAR DRAINAGE COLLECTION BAG
K872285 H-H HUNTER ACTIVE TENDON IMPLANT DC
K872284 H-H HUNTER ACTIVE TENDON IMPLANT PC
K872293 H-H HUNTER ACTIVE TENDON IMPLANT BC
K870660 H-H EXTERNAL VENTRICULAR DRAIN (EVD) COMP./SYSTEMS
K865075 H-H SUBGALEAL TROCAR
K853436 H-H HUNTER PASSIVE TENDON IMPLANT
K853437 H-H HUNTER TENDON ROD
K853438 H-H HUNTER ACTIVE TENDON IMPLANT
Search all 42 clearances from Holter-Hausner Intl. →