510(k) K852427

MANAN SPINAL NEEDLE by Manan Manufacturing Co., Inc. — Product Code GAA

K852427 is an FDA 510(k) premarket notification submitted by Manan Manufacturing Co., Inc. for the device "MANAN SPINAL NEEDLE". The FDA issued a decision of Substantially Equivalent on June 27, 1985. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Manan Manufacturing Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 27, 1985
Date Received
June 7, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Aspiration And Injection, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type