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

AUTOVAC

K Number: K921107 · Decision Sep 17, 1992
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
20
Review Days
192

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
AUTOVAC
K Number
K921107
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life Support Products, Inc.
Date Received
March 9, 1992
Decision Date
September 17, 1992
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

Similar 510(k) Clearances

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

View all

Other Clearances by Life Support Products, Inc.

K Number Device Name
K941870 LSPI AUTOMATIC VENTILATOR, MODEL AV2000-100
K941871 LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100
K940934 LIFE VAC
K936187 LSPI PRESSURE REGULATOR
K932200 LSPI AUTOMATIC VENTILATOR
K922819 INFANT DISPOSABLE BAG MASK RESUSCITATOR
K922691 LSP (MODEL 554) BAG MASK RESUSCITATOR
K932199 LSPI AUTOMATIC VENTILATOR, MODEL AV3000
K921553 LSPI INFANT BAG MASK
K924217 LSPI DISPOSABLE BAG MASK RESUSCITATOR/MODIFIED
Search all 20 clearances from Life Support Products, Inc. →