PACKING SPONGE
K-Number: K935911 · 1994-01-31
Advertisement
Device Summary
Frequently Asked Questions
What is the PACKING SPONGE?
PACKING SPONGE is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Mcneil Healthcare, Inc.. The 510(k) number is K935911.
When did PACKING SPONGE receive FDA 510(k) clearance?
PACKING SPONGE received FDA 510(k) clearance on 1994-01-31, under 510(k) number K935911.
Who is the listed applicant for PACKING SPONGE?
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 PACKING SPONGE?
The FDA product code for PACKING SPONGE 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.
Advertisement