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FDA 510(k)

DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP

K-Number: K884656 · 1988-11-25

ApplicantDermacare
Decision Date1988-11-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Dermacare. It received FDA 510(k) clearance on 1988-11-25 under 510(k) number K884656. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP?

DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP is a medical device that received FDA 510(k) clearance on 1988-11-25. The listed applicant is Dermacare. The 510(k) number is K884656.

When did DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP receive FDA 510(k) clearance?

DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP received FDA 510(k) clearance on 1988-11-25, under 510(k) number K884656.

Who is the listed applicant for DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP?

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 DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP?

The FDA product code for DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP is GEI.

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.

K893995DERMACARE TIE HOLDER

Related Devices (Code: GEI)

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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