PULSEMATE BX-5
K-Number: K874692 · 1988-02-02
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Device Summary
Frequently Asked Questions
What is the PULSEMATE BX-5?
PULSEMATE BX-5 is a medical device that received FDA 510(k) clearance on 1988-02-02. The listed applicant is Colin Medical Instruments Corp.. The 510(k) number is K874692.
When did PULSEMATE BX-5 receive FDA 510(k) clearance?
PULSEMATE BX-5 received FDA 510(k) clearance on 1988-02-02, under 510(k) number K874692.
Who is the listed applicant for PULSEMATE BX-5?
The FDA 510(k) record lists Colin Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PULSEMATE BX-5?
The FDA product code for PULSEMATE BX-5 is DQA.
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 Colin Medical Instruments 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.
Related Devices (Code: DQA)
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.
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