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FDA 510(k)

ASPEN DISPOSABLE BIPOLAR CORD

K-Number: K893732 · 1989-07-14

ApplicantConmedcorp
Decision Date1989-07-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ASPEN DISPOSABLE BIPOLAR CORD is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893732. 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 ASPEN DISPOSABLE BIPOLAR CORD?

ASPEN DISPOSABLE BIPOLAR CORD is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Conmedcorp. The 510(k) number is K893732.

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

ASPEN DISPOSABLE BIPOLAR CORD received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893732.

Who is the listed applicant for ASPEN DISPOSABLE BIPOLAR CORD?

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

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

The FDA product code for ASPEN DISPOSABLE BIPOLAR CORD is 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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