KEYMED KEY VAC SUCTION PUMP
K-Number: K820739 · 1982-05-21
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Device Summary
Frequently Asked Questions
What is the KEYMED KEY VAC SUCTION PUMP?
KEYMED KEY VAC SUCTION PUMP is a medical device that received FDA 510(k) clearance on 1982-05-21. The listed applicant is Keymed, Inc.. The 510(k) number is K820739.
When did KEYMED KEY VAC SUCTION PUMP receive FDA 510(k) clearance?
KEYMED KEY VAC SUCTION PUMP received FDA 510(k) clearance on 1982-05-21, under 510(k) number K820739.
Who is the listed applicant for KEYMED KEY VAC SUCTION PUMP?
The FDA 510(k) record lists Keymed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KEYMED KEY VAC SUCTION PUMP?
The FDA product code for KEYMED KEY VAC SUCTION PUMP is BTA.
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 Keymed, 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: BTA)
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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