PREAMP CABLE, MODEL B400-1011PA
K-Number: K003542 · 2001-04-06
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Device Summary
Frequently Asked Questions
What is the PREAMP CABLE, MODEL B400-1011PA?
PREAMP CABLE, MODEL B400-1011PA is a medical device that received FDA 510(k) clearance on 2001-04-06. The listed applicant is Beta Biomed Services, Inc.. The 510(k) number is K003542.
When did PREAMP CABLE, MODEL B400-1011PA receive FDA 510(k) clearance?
PREAMP CABLE, MODEL B400-1011PA received FDA 510(k) clearance on 2001-04-06, under 510(k) number K003542.
Who is the listed applicant for PREAMP CABLE, MODEL B400-1011PA?
The FDA 510(k) record lists Beta Biomed Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREAMP CABLE, MODEL B400-1011PA?
The FDA product code for PREAMP CABLE, MODEL B400-1011PA 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 Beta Biomed Services, 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.
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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