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FDA 510(k)

TECNOL COMPRESSION KNEE DRESSING

K-Number: K873368 · 1987-12-11

ApplicantTecnol New Jersey Wound Care, Inc.
Decision Date1987-12-11
Product CodeLLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TECNOL COMPRESSION KNEE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol New Jersey Wound Care, Inc.. It received FDA 510(k) clearance on 1987-12-11 under 510(k) number K873368. The device is classified under product code LLK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECNOL COMPRESSION KNEE DRESSING?

TECNOL COMPRESSION KNEE DRESSING is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K873368.

When did TECNOL COMPRESSION KNEE DRESSING receive FDA 510(k) clearance?

TECNOL COMPRESSION KNEE DRESSING received FDA 510(k) clearance on 1987-12-11, under 510(k) number K873368.

Who is the listed applicant for TECNOL COMPRESSION KNEE DRESSING?

The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECNOL COMPRESSION KNEE DRESSING?

The FDA product code for TECNOL COMPRESSION KNEE DRESSING is LLK.

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Other records listing Tecnol New Jersey Wound Care, 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.

K913043MODIFICATION TECNOL FLUIDSHIELD SURGICAL MASKSK911891FLUIDSHIELD(TM) CONE CLASSIC(TM) II SURGICAL MASKK911907FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VISK896193TECNOL LAZER(TM) SURGICAL MASKK894205TECNOL SILK STRIPK893702TECNOL GAITERS PRODUCT NUMBER 47725-010

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Related Devices (Code: LLK)

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.

K903532UNNA-SLEEVE(TM)Aci Medical, Inc.K871889COMPRESSION LEGGING DEVICEA-T Surgical Mfg. Co., Inc.K834460MODEL 1888 ALPHA COS/RESPIRATION CARSpacelabs, 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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