SITZMARKS

System, Gastrointestinal Motility (electrical)

LAFAYETTE PHARMACAL, INC.

The following data is part of a premarket notification filed by Lafayette Pharmacal, Inc. with the FDA for Sitzmarks.

Pre-market Notification Details

Device IDK881609
510k NumberK881609
Device Name:SITZMARKS
ClassificationSystem, Gastrointestinal Motility (electrical)
Applicant LAFAYETTE PHARMACAL, INC. 522 N. EARL AVE. Lafayette,  IN  47903
ContactRobert A Sharp
CorrespondentRobert A Sharp
LAFAYETTE PHARMACAL, INC. 522 N. EARL AVE. Lafayette,  IN  47903
Product CodeFFX  
CFR Regulation Number876.1725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-04-12
Decision Date1988-07-08

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00610858081306 K881609 000
00610858081016 K881609 000
00610858081023 K881609 000
00610858081078 K881609 000
00610858081085 K881609 000
00610858081092 K881609 000
00610858081108 K881609 000
00610858081115 K881609 000
00610858081122 K881609 000
00610858081139 K881609 000
00610858081009 K881609 000

Trademark Results [SITZMARKS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SITZMARKS
SITZMARKS
73695673 1492888 Live/Registered
LAFAYETTE PHARMACAL, INC.
1987-11-16

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