SUCTION CONNECTING TUBING
K-Number: K914601 · 1992-02-07
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Device Summary
Frequently Asked Questions
What is the SUCTION CONNECTING TUBING?
SUCTION CONNECTING TUBING is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Bemis Mfg. Co.. The 510(k) number is K914601.
When did SUCTION CONNECTING TUBING receive FDA 510(k) clearance?
SUCTION CONNECTING TUBING received FDA 510(k) clearance on 1992-02-07, under 510(k) number K914601.
Who is the listed applicant for SUCTION CONNECTING TUBING?
The FDA 510(k) record lists Bemis Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUCTION CONNECTING TUBING?
The FDA product code for SUCTION CONNECTING TUBING is GCX.
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 Bemis Mfg. Co. 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: GCX)
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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