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FDA 510(k)

SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY

K-Number: K883930 · 1988-11-09

ApplicantSeamed Corp.
Decision Date1988-11-09
Product CodeDTE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY is the device name listed in this FDA 510(k) record. The listed applicant is Seamed Corp.. It received FDA 510(k) clearance on 1988-11-09 under 510(k) number K883930. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY?

SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY is a medical device that received FDA 510(k) clearance on 1988-11-09. The listed applicant is Seamed Corp.. The 510(k) number is K883930.

When did SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY receive FDA 510(k) clearance?

SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY received FDA 510(k) clearance on 1988-11-09, under 510(k) number K883930.

Who is the listed applicant for SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY?

The FDA 510(k) record lists Seamed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY?

The FDA product code for SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY is DTE.

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Other records listing Seamed Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K923398CPI MODEL 2215K915364CHRONOCOR VI MODEL 5012K912507CPI MODEL 2215 & SEAMED MODEL 3400K910223CPI MODEL 2215/SEAMED MODEL 3400K872551SEAMED MODEL 3200K863903SEA MED MODEL 6000

View all 18 devices →

Related Devices (Code: DTE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241781Solo Pace ControlSolo Pace, Inc.K232721Lifetech Cardio Temporary PacemakerShenzhen Lifetech Cardio Medical Electronics Co., Ltd.K201011Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.K190825Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.K182839Lifetech Cardio Model 8301 Temporary PacemakerShenzhen Lifetech Cardio Medical Electronics Co., Ltd.K181973Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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