STERILIZATION WRAP
K-Number: K820521 · 1982-03-18
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Device Summary
Frequently Asked Questions
What is the STERILIZATION WRAP?
STERILIZATION WRAP is a medical device that received FDA 510(k) clearance on 1982-03-18. The listed applicant is General Medical Co.. The 510(k) number is K820521.
When did STERILIZATION WRAP receive FDA 510(k) clearance?
STERILIZATION WRAP received FDA 510(k) clearance on 1982-03-18, under 510(k) number K820521.
Who is the listed applicant for STERILIZATION WRAP?
The FDA 510(k) record lists General Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILIZATION WRAP?
The FDA product code for STERILIZATION WRAP is FRG.
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 General 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: FRG)
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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