FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

LORREX GAUZE SPONGES SPECIALTY

K Number: K942314 · Decision Jun 2, 1994
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
16
Review Days
20

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
LORREX GAUZE SPONGES SPECIALTY
K Number
K942314
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lorrex Health Products
Date Received
May 13, 1994
Decision Date
June 2, 1994
Product Code
EFQ
Advisory Committee
Unknown
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
EFQ Gauze/Sponge, Internal

Similar 510(k) Clearances

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

View all

Other Clearances by Lorrex Health Products

K Number Device Name
K945553 ROUND STICK SPONGES, FLAT STICK SPONGES
K945866 CYLINDRICAL SPONGE
K945333 KITTNER DISSECTOR
K945606 TRIANGULAR SPONGES
K945335 CHERRY DISSECTOR
K945334 CHERRY PIT DISSECTOR
K945332 ROSEBUD DISSECTOR
K945336 PEANUT DISSECTOR
K942824 LORREX IV SPONGES, STERILE 2'S; LORREX DRAIN SPONGES, STERILE 2'S
K942366 LORREX GAUZE SPONGES, X-RAY DETECTABLE
Search all 16 clearances from Lorrex Health Products →