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FDA 510(k)

BIOFILL BIOCELLULOSE DRESSING STERILE

K-Number: K950621 · 1995-12-26

ApplicantThe Purdue Frederick Co.
Decision Date1995-12-26
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIOFILL BIOCELLULOSE DRESSING STERILE is the device name listed in this FDA 510(k) record. The listed applicant is The Purdue Frederick Co.. It received FDA 510(k) clearance on 1995-12-26 under 510(k) number K950621. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOFILL BIOCELLULOSE DRESSING STERILE?

BIOFILL BIOCELLULOSE DRESSING STERILE is a medical device that received FDA 510(k) clearance on 1995-12-26. The listed applicant is The Purdue Frederick Co.. The 510(k) number is K950621.

When did BIOFILL BIOCELLULOSE DRESSING STERILE receive FDA 510(k) clearance?

BIOFILL BIOCELLULOSE DRESSING STERILE received FDA 510(k) clearance on 1995-12-26, under 510(k) number K950621.

Who is the listed applicant for BIOFILL BIOCELLULOSE DRESSING STERILE?

The FDA 510(k) record lists The Purdue Frederick Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOFILL BIOCELLULOSE DRESSING STERILE?

The FDA product code for BIOFILL BIOCELLULOSE DRESSING STERILE is KMF.

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Related Devices (Code: KMF)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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