BODAI SUCTION -SAFE 4
K-Number: K811241 · 1981-05-27
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Device Summary
Frequently Asked Questions
What is the BODAI SUCTION -SAFE 4?
BODAI SUCTION -SAFE 4 is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is Sontek Industries, Inc.. The 510(k) number is K811241.
When did BODAI SUCTION -SAFE 4 receive FDA 510(k) clearance?
BODAI SUCTION -SAFE 4 received FDA 510(k) clearance on 1981-05-27, under 510(k) number K811241.
Who is the listed applicant for BODAI SUCTION -SAFE 4?
The FDA 510(k) record lists Sontek Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BODAI SUCTION -SAFE 4?
The FDA product code for BODAI SUCTION -SAFE 4 is BSY.
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 Sontek Industries, 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: BSY)
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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