ASPIRATING TUBING
K-Number: K832519 · 1983-10-20
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Device Summary
Frequently Asked Questions
What is the ASPIRATING TUBING?
ASPIRATING TUBING is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Wells Johnson Co.. The 510(k) number is K832519.
When did ASPIRATING TUBING receive FDA 510(k) clearance?
ASPIRATING TUBING received FDA 510(k) clearance on 1983-10-20, under 510(k) number K832519.
Who is the listed applicant for ASPIRATING TUBING?
The FDA 510(k) record lists Wells Johnson Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASPIRATING TUBING?
The FDA product code for ASPIRATING TUBING is GAZ.
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 Wells Johnson Co. 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: GAZ)
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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