Medical Device Manufacturer · US , Walker , MI

Seamed Corp. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1982

Recent clearances: CPI MODEL 2215, CHRONOCOR VI MODEL 5012, CPI MODEL 2215 & SEAMED MODEL 3400

Total

Cleared

Denied

Seamed Corp. has 18 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.

Historical record: 18 cleared submissions from 1982 to 1992.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Seamed Corp. is one of 5811 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Seamed Corp.

18 devices

1-12 of 18

CHRONOCOR VI MODEL 5012

K915364 · DTE

Cardiovascular · 72d

Cleared Sep 03, 1991

CPI MODEL 2215 & SEAMED MODEL 3400

K912507 · DTE

Cardiovascular · 89d

Cleared Mar 19, 1991

CPI MODEL 2215/SEAMED MODEL 3400

K910223 · DTC

Cardiovascular · 60d

Cleared Nov 09, 1988

SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY

Cardiovascular · 194d

EXTERNAL PACEMAKER TELECTRONICS TE200

K852746 · JOQ

Cardiovascular · 77d

Cleared Jul 19, 1985

SEA MED DDD PACING SYSTEM ANALYZER

K851900 · DTC

Cardiovascular · 80d

Cleared Jul 16, 1985

CHRONOCOR V EXTERNAL PACER, MODEL 297A

K850822 · DTE

Cardiovascular · 138d

Seamed Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Seamed Corp.

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