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FDA 510(k)

STRYKER CONSTAVAC

K-Number: K823284 · 1983-01-14

ApplicantStryker Corp.
Decision Date1983-01-14
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER CONSTAVAC is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K823284. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER CONSTAVAC?

STRYKER CONSTAVAC is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Stryker Corp.. The 510(k) number is K823284.

When did STRYKER CONSTAVAC receive FDA 510(k) clearance?

STRYKER CONSTAVAC received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823284.

Who is the listed applicant for STRYKER CONSTAVAC?

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 CONSTAVAC?

The FDA product code for STRYKER CONSTAVAC is GCY.

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Other records listing Stryker Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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Related Devices (Code: GCY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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