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FDA 510(k)

SURGITEK DISPOSABLE BIPOLAR CORD

K-Number: K871910 · 1987-06-01

ApplicantDermacare Products, Inc.
Decision Date1987-06-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGITEK DISPOSABLE BIPOLAR CORD is the device name listed in this FDA 510(k) record. The listed applicant is Dermacare Products, Inc.. It received FDA 510(k) clearance on 1987-06-01 under 510(k) number K871910. 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 SURGITEK DISPOSABLE BIPOLAR CORD?

SURGITEK DISPOSABLE BIPOLAR CORD is a medical device that received FDA 510(k) clearance on 1987-06-01. The listed applicant is Dermacare Products, Inc.. The 510(k) number is K871910.

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

SURGITEK DISPOSABLE BIPOLAR CORD received FDA 510(k) clearance on 1987-06-01, under 510(k) number K871910.

Who is the listed applicant for SURGITEK DISPOSABLE BIPOLAR CORD?

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

What is the FDA product code for SURGITEK DISPOSABLE BIPOLAR CORD?

The FDA product code for SURGITEK DISPOSABLE BIPOLAR CORD is GEI.

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Other records listing Dermacare Products, Inc. as applicant

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Related Devices (Code: GEI)

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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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