CP & S STERILE BURN SHEET
K-Number: K930759 · 1994-01-21
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Device Summary
Frequently Asked Questions
What is the CP & S STERILE BURN SHEET?
CP & S STERILE BURN SHEET is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Consolidated Products & Services, Inc.. The 510(k) number is K930759.
When did CP & S STERILE BURN SHEET receive FDA 510(k) clearance?
CP & S STERILE BURN SHEET received FDA 510(k) clearance on 1994-01-21, under 510(k) number K930759.
Who is the listed applicant for CP & S STERILE BURN SHEET?
The FDA 510(k) record lists Consolidated Products & Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CP & S STERILE BURN SHEET?
The FDA product code for CP & S STERILE BURN SHEET is FPY.
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 Consolidated Products & Services, Inc. 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: FPY)
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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