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FDA 510(k)

BIO-POLAR FORCEPS

K-Number: K915826 · 1992-06-02

ApplicantApplied Medical
Decision Date1992-06-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIO-POLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical. It received FDA 510(k) clearance on 1992-06-02 under 510(k) number K915826. 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 BIO-POLAR FORCEPS?

BIO-POLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1992-06-02. The listed applicant is Applied Medical. The 510(k) number is K915826.

When did BIO-POLAR FORCEPS receive FDA 510(k) clearance?

BIO-POLAR FORCEPS received FDA 510(k) clearance on 1992-06-02, under 510(k) number K915826.

Who is the listed applicant for BIO-POLAR FORCEPS?

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

What is the FDA product code for BIO-POLAR FORCEPS?

The FDA product code for BIO-POLAR FORCEPS is GEI.

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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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