510(k) K935881

SPECIALTY SPONGES by Mcneil Healthcare, Inc. — Product Code GDY

K935881 is an FDA 510(k) premarket notification submitted by Mcneil Healthcare, Inc. for the device "SPECIALTY SPONGES". The FDA issued a decision of Substantially Equivalent on Jan 31, 1994. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. Mcneil Healthcare, Inc. has 18 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Jan 31, 1994
Date Received
Dec 9, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device classification

Device Name
Gauze/Sponge, Internal, X-Ray Detectable
Device Class
Class I
Regulation Number
878.4450
Review Panel
SU
Submission Type
510(k) Exempt

Source: FDA 510(k) database entry for K935881. Report a data issue: hello@regdatalab.com.