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

NEBULIZER PUMP, POWERED MODEL 1180

K Number: K925011 · Decision Jan 12, 1994
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
73
Applicant Total
9
Review Days
467

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
NEBULIZER PUMP, POWERED MODEL 1180
K Number
K925011
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.6250
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thomas Industries
Date Received
October 2, 1992
Decision Date
January 12, 1994
Product Code
BTI
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
BTI Compressor, Air, Portable

Similar 510(k) Clearances

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

View all

Other Clearances by Thomas Industries

K Number Device Name
K041199 MEDI-PUMP ASPIRATOR, MODEL 1615
K965059 CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243)
K952806 MEDI PUMP ASPIRATOR MODELS 1130 AND 1135
K950290 MEDI - PUMP
K951729 MEDI - PUMP
K950867 MEDI - PUMP
K944399 MEDI-PUMP
K925010 NEBULIZER PUMP, POWERED, MODEL 1110