SUCTION INSTRUMENT, MACBICK POOLE TIP
K-Number: K760216 · 1976-08-23
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Device Summary
Frequently Asked Questions
What is the SUCTION INSTRUMENT, MACBICK POOLE TIP?
SUCTION INSTRUMENT, MACBICK POOLE TIP is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K760216.
When did SUCTION INSTRUMENT, MACBICK POOLE TIP receive FDA 510(k) clearance?
SUCTION INSTRUMENT, MACBICK POOLE TIP received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760216.
Who is the listed applicant for SUCTION INSTRUMENT, MACBICK POOLE TIP?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUCTION INSTRUMENT, MACBICK POOLE TIP?
The FDA product code for SUCTION INSTRUMENT, MACBICK POOLE TIP 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 C.R. Bard, 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: 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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