510(k) K964921

BASIC BIOPSY TRAY. DISPOSABLE, STERILE by Trinity Laboratories, Inc. — Product Code LRO

K964921 is an FDA 510(k) premarket notification submitted by Trinity Laboratories, Inc. for the device "BASIC BIOPSY TRAY. DISPOSABLE, STERILE". The FDA issued a decision of Substantially Equivalent on January 22, 1997. The device falls under product code LRO (General Surgery Tray), a Class II device regulated under 21 CFR 878.4370. Trinity Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 1997
Date Received
December 9, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
General Surgery Tray
Device Class
Class II
Regulation Number
878.4370
Review Panel
SU
Submission Type

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance