510(k) K822525

LARYNGOSCOPES RIGID by Kelleher Corp. — Product Code EQN

K822525 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "LARYNGOSCOPES RIGID". The FDA issued a decision of Substantially Equivalent on September 9, 1982. The device falls under product code EQN (Laryngoscope, Nasopharyngoscope), a Class II device regulated under 21 CFR 874.4760. Kelleher Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 1982
Date Received
August 23, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Laryngoscope, Nasopharyngoscope
Device Class
Class II
Regulation Number
874.4760
Review Panel
EN
Submission Type

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).