SUCTION PROBE
K-Number: K803206 · 1981-01-21
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Device Summary
Frequently Asked Questions
What is the SUCTION PROBE?
SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1981-01-21. The listed applicant is Bemis Health Care. The 510(k) number is K803206.
When did SUCTION PROBE receive FDA 510(k) clearance?
SUCTION PROBE received FDA 510(k) clearance on 1981-01-21, under 510(k) number K803206.
Who is the listed applicant for SUCTION PROBE?
The FDA 510(k) record lists Bemis Health Care as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUCTION PROBE?
The FDA product code for SUCTION PROBE is JOL.
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 Health Care 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: JOL)
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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