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

PATIENT EXAMINATION GLOVES (LATEX)

K Number: K891649 · Decision Apr 4, 1989
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
17
Review Days
18

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
PATIENT EXAMINATION GLOVES (LATEX)
K Number
K891649
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Lic-Orthion
Date Received
March 17, 1989
Decision Date
April 4, 1989
Product Code
LYY
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LYY Latex Patient Examination Glove

Similar 510(k) Clearances

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

View all

Other Clearances by Lic-Orthion

K Number Device Name
K862022 LIC-ORTHION MULTI-THERAPY TREATMENT TABLE
K854730 DAISY (ABSORBENT INCONTINENCE SHIELD)
K854729 ADAM (ABSORBENT INCONTINENCE SHIELD)
K851470 BIBAG, BIBAND & BIFIX - SINGLE USE URINE COLLECTOR
K851471 TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR
K843233 ANATOM SYSTEM
K843234 CITOMAT AUTOCLAVES
K830853 LAVATORY SEAT HEIGHTENER
K830849 OB TILT
K830854 COLLAPSABLE LAVATORY SEAT HEIGHTENER
Search all 17 clearances from Lic-Orthion →