RAPIDO-LASTIC IN STERILE FORM
K-Number: K821701 · 1982-07-22
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Device Summary
Frequently Asked Questions
What is the RAPIDO-LASTIC IN STERILE FORM?
RAPIDO-LASTIC IN STERILE FORM is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Conco Medical Co.. The 510(k) number is K821701.
When did RAPIDO-LASTIC IN STERILE FORM receive FDA 510(k) clearance?
RAPIDO-LASTIC IN STERILE FORM received FDA 510(k) clearance on 1982-07-22, under 510(k) number K821701.
Who is the listed applicant for RAPIDO-LASTIC IN STERILE FORM?
The FDA 510(k) record lists Conco Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAPIDO-LASTIC IN STERILE FORM?
The FDA product code for RAPIDO-LASTIC IN STERILE FORM is EFQ.
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 Conco Medical 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: EFQ)
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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