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FDA 510(k)

STRYKER ENCORE STERILIZER

K-Number: K962755 · 1997-03-04

ApplicantStryker Corp.
Decision Date1997-03-04
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER ENCORE STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1997-03-04 under 510(k) number K962755. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER ENCORE STERILIZER?

STRYKER ENCORE STERILIZER is a medical device that received FDA 510(k) clearance on 1997-03-04. The listed applicant is Stryker Corp.. The 510(k) number is K962755.

When did STRYKER ENCORE STERILIZER receive FDA 510(k) clearance?

STRYKER ENCORE STERILIZER received FDA 510(k) clearance on 1997-03-04, under 510(k) number K962755.

Who is the listed applicant for STRYKER ENCORE STERILIZER?

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 STRYKER ENCORE STERILIZER?

The FDA product code for STRYKER ENCORE STERILIZER is FLE.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: FLE)

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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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