TYGON PAC-STOPCOCKS
K-Number: K770708 · 1977-06-08
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Device Summary
Frequently Asked Questions
What is the TYGON PAC-STOPCOCKS?
TYGON PAC-STOPCOCKS is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K770708.
When did TYGON PAC-STOPCOCKS receive FDA 510(k) clearance?
TYGON PAC-STOPCOCKS received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770708.
Who is the listed applicant for TYGON PAC-STOPCOCKS?
The FDA 510(k) record lists Norton Performance Plastics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TYGON PAC-STOPCOCKS?
The FDA product code for TYGON PAC-STOPCOCKS is FMG.
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 Norton Performance Plastics Corp. 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: FMG)
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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