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

LINE CADDY

K Number: K810294 · Decision Feb 26, 1981
Classifications
1
FEI Numbers
373
Registration Numbers
373
Same Product Code
14
Applicant Total
10
Review Days
22

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
LINE CADDY
K Number
K810294
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Instranetics, Inc.
Date Received
February 4, 1981
Decision Date
February 26, 1981
Product Code
HXB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HXB Probe

Similar 510(k) Clearances

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

View all

Other Clearances by Instranetics, Inc.

K Number Device Name
K823430 INSTRA-SAFE
K811824 CAUTERY CADDY PAD
K811823 SHARPS CADDY FB
K811822 TIP-VU
K810208 BLADE SAFE
K802865 SAFE T COUNT
K802866 SHARPS CADDY MAGNETIC & SHARPS CADDY FOA
K781575 DISPOSABLE LYMPHANGIOGRAM SET
K770894 NEURO-SORB PATTIES