510(k) K792247

TAYLOR PATIENT TRANSFER BOARD by Taylor Medical Equipment — Product Code IKX

K792247 is an FDA 510(k) premarket notification submitted by Taylor Medical Equipment for the device "TAYLOR PATIENT TRANSFER BOARD". The FDA issued a decision of Substantially Equivalent on November 30, 1979. The device falls under product code IKX (Aid, Transfer), a Class I device regulated under 21 CFR 890.5050. Taylor Medical Equipment has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 1979
Date Received
November 7, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Aid, Transfer
Device Class
Class I
Regulation Number
890.5050
Review Panel
PM
Submission Type