510(k) K781371

BONE MARROW ASPIRATION KIT by Ferris Mfg. Corp. — Product Code GAA

K781371 is an FDA 510(k) premarket notification submitted by Ferris Mfg. Corp. for the device "BONE MARROW ASPIRATION KIT". The FDA issued a decision of Substantially Equivalent on September 20, 1978. The device falls under product code GAA (Needle, Aspiration And Injection, Disposable), a Class I device regulated under 21 CFR 878.4800. Ferris Mfg. Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 20, 1978
Date Received
August 8, 1978
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