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FDA 510(k)

ALGINATE WOOL FIBER

K-Number: K870383 · 1987-04-30

ApplicantAdri
Decision Date1987-04-30
Product CodeKHR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ALGINATE WOOL FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Adri. It received FDA 510(k) clearance on 1987-04-30 under 510(k) number K870383. The device is classified under product code KHR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALGINATE WOOL FIBER?

ALGINATE WOOL FIBER is a medical device that received FDA 510(k) clearance on 1987-04-30. The listed applicant is Adri. The 510(k) number is K870383.

When did ALGINATE WOOL FIBER receive FDA 510(k) clearance?

ALGINATE WOOL FIBER received FDA 510(k) clearance on 1987-04-30, under 510(k) number K870383.

Who is the listed applicant for ALGINATE WOOL FIBER?

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

What is the FDA product code for ALGINATE WOOL FIBER?

The FDA product code for ALGINATE WOOL FIBER is KHR.

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.

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Other records listing Adri 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.

K041268SILVERSITE OR CALGITROLK011618CALGITROL AG SILVER ALGINATE WOUND DRESSINGK000054FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGENK963656FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSINGK940404ALGINATE FIBER TOPICAL WOUND DRESSING

Related Devices (Code: KHR)

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.

K980783SIMPLEX SALIVA ABSORBER/COLLECTOR, MODEL SSA-5Irt Management Corp.K954068GENERAL HYGIENE KITPhysician Industries, Inc.K953812GAUZE SPONGERemington Medical, Inc.K891054NON-STERILE GAUZE SPONGEDispomed, Inc.K891354ORTHODONTIC COTTON ROLL HOLDERSAmerican OrthodonticsK890734DRY TIPSMicrocopy, Div. Neo-Flo, Inc.

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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