SRH-678 VACCUUM TUBING
K-Number: K920210 · 1992-10-01
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Device Summary
Frequently Asked Questions
What is the SRH-678 VACCUUM TUBING?
SRH-678 VACCUUM TUBING is a medical device that received FDA 510(k) clearance on 1992-10-01. The listed applicant is Quinn Healthcare Products. The 510(k) number is K920210.
When did SRH-678 VACCUUM TUBING receive FDA 510(k) clearance?
SRH-678 VACCUUM TUBING received FDA 510(k) clearance on 1992-10-01, under 510(k) number K920210.
Who is the listed applicant for SRH-678 VACCUUM TUBING?
The FDA 510(k) record lists Quinn Healthcare Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SRH-678 VACCUUM TUBING?
The FDA product code for SRH-678 VACCUUM TUBING is FYD.
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 Quinn Healthcare Products 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: FYD)
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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