STOCKINETTE
K-Number: K770173 · 1977-02-08
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Device Summary
Frequently Asked Questions
What is the STOCKINETTE?
STOCKINETTE is a medical device that received FDA 510(k) clearance on 1977-02-08. The listed applicant is Chase Mfg. Co.. The 510(k) number is K770173.
When did STOCKINETTE receive FDA 510(k) clearance?
STOCKINETTE received FDA 510(k) clearance on 1977-02-08, under 510(k) number K770173.
Who is the listed applicant for STOCKINETTE?
The FDA 510(k) record lists Chase Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOCKINETTE?
The FDA product code for STOCKINETTE is ILG.
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 Chase Mfg. 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: ILG)
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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