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FDA 510(k)

GAS PLASMA STERILIZATION

K-Number: K972774 · 1999-05-05

ApplicantZimmer, Inc.
Decision Date1999-05-05
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GAS PLASMA STERILIZATION is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1999-05-05 under 510(k) number K972774. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS PLASMA STERILIZATION?

GAS PLASMA STERILIZATION is a medical device that received FDA 510(k) clearance on 1999-05-05. The listed applicant is Zimmer, Inc.. The 510(k) number is K972774.

When did GAS PLASMA STERILIZATION receive FDA 510(k) clearance?

GAS PLASMA STERILIZATION received FDA 510(k) clearance on 1999-05-05, under 510(k) number K972774.

Who is the listed applicant for GAS PLASMA STERILIZATION?

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

What is the FDA product code for GAS PLASMA STERILIZATION?

The FDA product code for GAS PLASMA STERILIZATION is JWH.

Related Clinical Trials

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.

Other records listing Zimmer, Inc. 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.

View all 344 devices →

Related Devices (Code: JWH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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