CATHETERS, GREENLINE SUCTION
K-Number: K790606 · 1979-04-23
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Device Summary
Frequently Asked Questions
What is the CATHETERS, GREENLINE SUCTION?
CATHETERS, GREENLINE SUCTION is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Snyder Laboratories, Inc.. The 510(k) number is K790606.
When did CATHETERS, GREENLINE SUCTION receive FDA 510(k) clearance?
CATHETERS, GREENLINE SUCTION received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790606.
Who is the listed applicant for CATHETERS, GREENLINE SUCTION?
The FDA 510(k) record lists Snyder Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETERS, GREENLINE SUCTION?
The FDA product code for CATHETERS, GREENLINE SUCTION 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 Snyder Laboratories, 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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