BURN COMPRESS
K-Number: K935932 · 1994-01-14
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Device Summary
Frequently Asked Questions
What is the BURN COMPRESS?
BURN COMPRESS is a medical device that received FDA 510(k) clearance on 1994-01-14. The listed applicant is Mcneil Healthcare, Inc.. The 510(k) number is K935932.
When did BURN COMPRESS receive FDA 510(k) clearance?
BURN COMPRESS received FDA 510(k) clearance on 1994-01-14, under 510(k) number K935932.
Who is the listed applicant for BURN COMPRESS?
The FDA 510(k) record lists Mcneil Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BURN COMPRESS?
The FDA product code for BURN COMPRESS 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 Mcneil Healthcare, 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: 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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