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FDA 510(k)

FASSIRE-DUVAL TELESCOPIC IM SYSTEM

K-Number: K020885 · 2003-02-06

ApplicantPega Medical, Inc.
Decision Date2003-02-06
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FASSIRE-DUVAL TELESCOPIC IM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pega Medical, Inc.. It received FDA 510(k) clearance on 2003-02-06 under 510(k) number K020885. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FASSIRE-DUVAL TELESCOPIC IM SYSTEM?

FASSIRE-DUVAL TELESCOPIC IM SYSTEM is a medical device that received FDA 510(k) clearance on 2003-02-06. The listed applicant is Pega Medical, Inc.. The 510(k) number is K020885.

When did FASSIRE-DUVAL TELESCOPIC IM SYSTEM receive FDA 510(k) clearance?

FASSIRE-DUVAL TELESCOPIC IM SYSTEM received FDA 510(k) clearance on 2003-02-06, under 510(k) number K020885.

Who is the listed applicant for FASSIRE-DUVAL TELESCOPIC IM SYSTEM?

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

What is the FDA product code for FASSIRE-DUVAL TELESCOPIC IM SYSTEM?

The FDA product code for FASSIRE-DUVAL TELESCOPIC IM SYSTEM is HSB.

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Related Devices (Code: HSB)

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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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