510(k) K831901

LACIMAL INTUBATION SETS by Visitec Co. — Product Code HNL

K831901 is an FDA 510(k) premarket notification submitted by Visitec Co. for the device "LACIMAL INTUBATION SETS". The FDA issued a decision of Substantially Equivalent on July 12, 1983. The device falls under product code HNL (Probe, Lachrymal), a Class I device regulated under 21 CFR 886.4350. Visitec Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 12, 1983
Date Received
June 14, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Probe, Lachrymal
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type