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FDA 510(k)

PYRAMID

K-Number: K982645 · 1998-09-02

ApplicantBisco, Inc.
Decision Date1998-09-02
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PYRAMID is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1998-09-02 under 510(k) number K982645. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PYRAMID?

PYRAMID is a medical device that received FDA 510(k) clearance on 1998-09-02. The listed applicant is Bisco, Inc.. The 510(k) number is K982645.

When did PYRAMID receive FDA 510(k) clearance?

PYRAMID received FDA 510(k) clearance on 1998-09-02, under 510(k) number K982645.

Who is the listed applicant for PYRAMID?

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

What is the FDA product code for PYRAMID?

The FDA product code for PYRAMID is EBF.

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Other records listing Bisco, Inc. as applicant

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Related Devices (Code: EBF)

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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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