EASYGO ASPIRATOR
K-Number: K971749 · 1998-04-01
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Device Summary
Frequently Asked Questions
What is the EASYGO ASPIRATOR?
EASYGO ASPIRATOR is a medical device that received FDA 510(k) clearance on 1998-04-01. The listed applicant is Precision Medical, Inc.. The 510(k) number is K971749.
When did EASYGO ASPIRATOR receive FDA 510(k) clearance?
EASYGO ASPIRATOR received FDA 510(k) clearance on 1998-04-01, under 510(k) number K971749.
Who is the listed applicant for EASYGO ASPIRATOR?
The FDA 510(k) record lists Precision Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EASYGO ASPIRATOR?
The FDA product code for EASYGO ASPIRATOR 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 Precision Medical, 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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