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

ASTECH PEAK FLOW METER

K Number: K954277 · Decision Feb 21, 1996
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
79
Applicant Total
2
Review Days
163

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
ASTECH PEAK FLOW METER
K Number
K954277
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Center Laboratories, Inc.
Date Received
September 11, 1995
Decision Date
February 21, 1996
Product Code
BZH
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
BZH Meter, Peak Flow, Spirometry

Similar 510(k) Clearances

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

View all

Other Clearances by Center Laboratories, Inc.

K Number Device Name
K844230 RHINOMANOMETER A440 DIGITAL