FIELD SUCTION DISSECTOR
K-Number: K803292 · 1981-01-29
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Device Summary
Frequently Asked Questions
What is the FIELD SUCTION DISSECTOR?
FIELD SUCTION DISSECTOR is a medical device that received FDA 510(k) clearance on 1981-01-29. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K803292.
When did FIELD SUCTION DISSECTOR receive FDA 510(k) clearance?
FIELD SUCTION DISSECTOR received FDA 510(k) clearance on 1981-01-29, under 510(k) number K803292.
Who is the listed applicant for FIELD SUCTION DISSECTOR?
The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIELD SUCTION DISSECTOR?
The FDA product code for FIELD SUCTION DISSECTOR is GDI.
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 V. Mueller O.V. Baxter Healthcare Corp. 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: GDI)
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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