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FDA 510(k)

PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS

K-Number: K932892 · 1994-07-06

ApplicantSiemens-Pacesetter, Inc.
Decision Date1994-07-06
Product CodeDTB
Advisory CommitteeCV
DecisionUnknown

Device Summary

PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens-Pacesetter, Inc.. It received FDA 510(k) clearance on 1994-07-06 under 510(k) number K932892. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS?

PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS is a medical device that received FDA 510(k) clearance on 1994-07-06. The listed applicant is Siemens-Pacesetter, Inc.. The 510(k) number is K932892.

When did PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS receive FDA 510(k) clearance?

PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS received FDA 510(k) clearance on 1994-07-06, under 510(k) number K932892.

Who is the listed applicant for PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS?

The FDA 510(k) record lists Siemens-Pacesetter, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS?

The FDA product code for PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS is DTB.

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Other records listing Siemens-Pacesetter, Inc. 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.

K942440AFP CARDIAC PACING SYSTEM MODEL 283K925038PACING LEAD MODEL 1188TK930876SILICONE BIPOLAR LEAD MODELS 1136T, 1142T &1146TK925347MODEL 1148T TRANSVENOUS, SCREW-IN LEADK920822CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODEK921318ADAPTING SLEEVE KIT MODEL 4023

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Related Devices (Code: DTB)

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.

K061212BIOTRONIK ENDOCARDIAL PACING LEADSBiotronik, Inc.K041809PERMANENT PACING LEAD, MODEL PY2Oscor, Inc.K040569PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJUOscor, Inc.K031274MODEL 5071 MYOCARDIAL PACING LEADMedtronic VascularK031210MODEL 4951M MYOCARDIAL UNIPOLAR LEADMetronic, Inc.K023205ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BPBiotronik, 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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