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

CORRUGATED FLEX TUBING

K Number: K810362 · Decision Mar 17, 1981
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
61
Applicant Total
11
Review Days
34

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
CORRUGATED FLEX TUBING
K Number
K810362
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Todd Industries, Inc.
Date Received
February 11, 1981
Decision Date
March 17, 1981
Product Code
BYX
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
BYX Tubing, Pressure And Accessories

Similar 510(k) Clearances

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

View all

Other Clearances by Todd Industries, Inc.

K Number Device Name
K810343 NEBULIZERS
K810342 NASAL CANNULA
K810340 ADULT MASKS & PEDIATRIC MASKS
K810373 VENTURI MASK/DELIVERY SYSTEM #'S
K810361 CONNECTOR ADAPTERS
K810344 OXYGEN TUBING
K810341 LIFELINE IPPB SET-UP
K810339 NOSECLIP #6118
K810430 VENTURI MASK/DELIVERY SYSTEM #6078
K810374 CORRUGATED FLEX TUBING #6000,
Search all 11 clearances from Todd Industries, Inc. →