BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM
K-Number: K060277 · 2006-03-03
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Device Summary
Frequently Asked Questions
What is the BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM?
BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM is a medical device that received FDA 510(k) clearance on 2006-03-03. The listed applicant is Boehringer Laboratories. The 510(k) number is K060277.
When did BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM receive FDA 510(k) clearance?
BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM received FDA 510(k) clearance on 2006-03-03, under 510(k) number K060277.
Who is the listed applicant for BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM?
The FDA 510(k) record lists Boehringer Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM?
The FDA product code for BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM is JCX.
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 Boehringer Laboratories 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: JCX)
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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