BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000
K-Number: K983228 · 1999-03-15
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Device Summary
Frequently Asked Questions
What is the BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000?
BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000 is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is Murray Electronics. The 510(k) number is K983228.
When did BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000 receive FDA 510(k) clearance?
BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000 received FDA 510(k) clearance on 1999-03-15, under 510(k) number K983228.
Who is the listed applicant for BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000?
The FDA 510(k) record lists Murray Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000?
The FDA product code for BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000 is NYN.
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 Murray Electronics 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: NYN)
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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