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FDA 510(k)

BIOBLANKET

K-Number: K041923 · 2004-09-08

ApplicantKensey Nash Corp.
Decision Date2004-09-08
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIOBLANKET is the device name listed in this FDA 510(k) record. The listed applicant is Kensey Nash Corp.. It received FDA 510(k) clearance on 2004-09-08 under 510(k) number K041923. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOBLANKET?

BIOBLANKET is a medical device that received FDA 510(k) clearance on 2004-09-08. The listed applicant is Kensey Nash Corp.. The 510(k) number is K041923.

When did BIOBLANKET receive FDA 510(k) clearance?

BIOBLANKET received FDA 510(k) clearance on 2004-09-08, under 510(k) number K041923.

Who is the listed applicant for BIOBLANKET?

The FDA 510(k) record lists Kensey Nash Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOBLANKET?

The FDA product code for BIOBLANKET is FTM.

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Other records listing Kensey Nash Corp. 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.

K103787MEDEOR MATRIXK091192KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XXK091499MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)K090919KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANEK073519QUICKCAT EXTRACTION CATHETER, MODEL 60090-01K071695KENSEY NASH MACROPORE SHIELD

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Related Devices (Code: FTM)

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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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