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FDA 510(k)

PAINPUMP1; PAINPUMP2

K-Number: K042405 · 2004-10-14

ApplicantStryker Corp.
Decision Date2004-10-14
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PAINPUMP1; PAINPUMP2 is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2004-10-14 under 510(k) number K042405. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAINPUMP1; PAINPUMP2?

PAINPUMP1; PAINPUMP2 is a medical device that received FDA 510(k) clearance on 2004-10-14. The listed applicant is Stryker Corp.. The 510(k) number is K042405.

When did PAINPUMP1; PAINPUMP2 receive FDA 510(k) clearance?

PAINPUMP1; PAINPUMP2 received FDA 510(k) clearance on 2004-10-14, under 510(k) number K042405.

Who is the listed applicant for PAINPUMP1; PAINPUMP2?

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

What is the FDA product code for PAINPUMP1; PAINPUMP2?

The FDA product code for PAINPUMP1; PAINPUMP2 is FRN.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: FRN)

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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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