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

AUGUSTINE FIBEROPTIC LARYNGOSCOPE

K Number: K915161 · Decision May 29, 1992
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
63
Applicant Total
25
Review Days
197

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
AUGUSTINE FIBEROPTIC LARYNGOSCOPE
K Number
K915161
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5540
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Augustine Medical, Inc.
Date Received
November 14, 1991
Decision Date
May 29, 1992
Product Code
CCW
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
CCW Laryngoscope, Rigid

Similar 510(k) Clearances

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

View all

Other Clearances by Augustine Medical, Inc.

K Number Device Name
K021473 BAIR HUGGER TEMPERATURE MANAGEMENT SYSTEM
K020077 MODIFICATION TO AUGUSTINE MEDICAL WOUND CARE SYSTEM, MODEL 68XXX
K001149 AUGUSTINE MEDICAL BAIR HUUGER, MODEL 750 TOTAL TEMPERATURE MANAGEMENT SYSTEM-(MODEL 750 WARMING UNIT, BAIR HUGGER BLANK
K973741 BAIR HUGGER BLOOD/FLUID WARMER
K964673 BAIR HUGGER MODEL 630 CARDIAC BLANKET
K963293 AUGUSTINE MEDICAL WOUND CARE SYSTEM MODEL 68XXX
K963672 MODEL 90022 ROLLING STAND
K960167 SYSTEM, THERMAL REGULATING 74-DWJ
K954446 AUGUSTINE INTUBATION GUIDE
K952864 BAIR HUGGER MODEL 655 BLANKET
Search all 25 clearances from Augustine Medical, Inc. →