Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS

K-Number: K890547 · 1989-03-22

Decision Date1989-03-22
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS is the device name listed in this FDA 510(k) record. The listed applicant is Pacesetter Systems. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K890547. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS?

SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Pacesetter Systems. The 510(k) number is K890547.

When did SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS receive FDA 510(k) clearance?

SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS received FDA 510(k) clearance on 1989-03-22, under 510(k) number K890547.

Who is the listed applicant for SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS?

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

What is the FDA product code for SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS?

The FDA product code for SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS is DTB.

Related Clinical Trials

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.

Other records listing Pacesetter Systems 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.

View all 96 devices →

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.

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.

↑