Medical Device Manufacturer · US , Walker , MI

Diag Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1980

Total

Cleared

Denied

Diag Corp. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1980 to 1999. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Diag Corp. Filter by specialty or product code using the sidebar.

Diag Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Diag Corp.

9 devices

1-9 of 9

Cleared Mar 24, 1999

SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229

K984062 · DYB

Cardiovascular · 128d

Cleared Nov 29, 1991

DAIG FAST CATH(TM) TRANSSEPTAL SHEATH INTRODUCER

K911883 · DYB

Cardiovascular · 214d

Cleared May 07, 1991

DISPOSABLE PATIENT CABLE

K910645 · DSA

Cardiovascular · 83d

Cleared Sep 17, 1985

ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIP

K852446 · DTB

Cardiovascular · 99d

Cleared Mar 26, 1982

CARDIOVASCULAR TEMP. PACEMAKER ELEC

K820003 · LDF

Cardiovascular · 81d

Cleared Mar 12, 1982

PERMANENT & TEMPORARY PACEMAKER ELECTR.

K820262 · DTB

Cardiovascular · 38d

Cleared Feb 04, 1982

PERMANENT ENDOCARD. UNIPOLAR TINED LEAD

K812905 · DTB

Cardiovascular · 108d

Cleared Sep 16, 1981

PERM. ENDOCARDIAL UNIPOLAR TINED ATRIAL

K812270 · DTB

Cardiovascular · 34d

Cleared May 28, 1980

ENDOCARD. PACING LEAD LONG LENGTH PL200

K800349 · DTB

Cardiovascular · 103d

Diag Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Diag Corp.

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