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FDA 510(k)

DERMACARE TIE HOLDER

K-Number: K893995 · 1989-08-11

ApplicantDermacare
Decision Date1989-08-11
Product CodeKGS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMACARE TIE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Dermacare. It received FDA 510(k) clearance on 1989-08-11 under 510(k) number K893995. The device is classified under product code KGS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMACARE TIE HOLDER?

DERMACARE TIE HOLDER is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is Dermacare. The 510(k) number is K893995.

When did DERMACARE TIE HOLDER receive FDA 510(k) clearance?

DERMACARE TIE HOLDER received FDA 510(k) clearance on 1989-08-11, under 510(k) number K893995.

Who is the listed applicant for DERMACARE TIE HOLDER?

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

What is the FDA product code for DERMACARE TIE HOLDER?

The FDA product code for DERMACARE TIE HOLDER is KGS.

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 Dermacare 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.

K884656DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP

Related Devices (Code: KGS)

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.

K030031SOFT TISSUE ANCHORING WASHERSAccu-Speed, IncorporatedK020480RBMSmith & Nephew, Inc.K964935SUTURE LOCKSmith & Nephew Endoscopy, Inc.K941740ACUFEX ROTATOR CUFF FIXATION BUTTONAcufex Microsurgical, Inc.K930675MITEK CONE WASHERMitek Surgical Products, Inc.K904435VENTROFIL TENSION RELIEF SUTURE SETAesculap, 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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