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FDA 510(k)

LEAD STYLET,MODELS 6505,6506,6507,6508

K-Number: K992863 · 1999-11-12

ApplicantGuidant Corp.
Decision Date1999-11-12
Product CodeDRB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEAD STYLET,MODELS 6505,6506,6507,6508 is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corp.. It received FDA 510(k) clearance on 1999-11-12 under 510(k) number K992863. The device is classified under product code DRB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEAD STYLET,MODELS 6505,6506,6507,6508?

LEAD STYLET,MODELS 6505,6506,6507,6508 is a medical device that received FDA 510(k) clearance on 1999-11-12. The listed applicant is Guidant Corp.. The 510(k) number is K992863.

When did LEAD STYLET,MODELS 6505,6506,6507,6508 receive FDA 510(k) clearance?

LEAD STYLET,MODELS 6505,6506,6507,6508 received FDA 510(k) clearance on 1999-11-12, under 510(k) number K992863.

Who is the listed applicant for LEAD STYLET,MODELS 6505,6506,6507,6508?

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

What is the FDA product code for LEAD STYLET,MODELS 6505,6506,6507,6508?

The FDA product code for LEAD STYLET,MODELS 6505,6506,6507,6508 is DRB.

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Related Devices (Code: DRB)

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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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