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FDA 510(k)

GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM

K-Number: K962687 · 1997-03-28

Decision Date1997-03-28
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nichols Institute Diagnostics. It received FDA 510(k) clearance on 1997-03-28 under 510(k) number K962687. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM?

GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM is a medical device that received FDA 510(k) clearance on 1997-03-28. The listed applicant is Nichols Institute Diagnostics. The 510(k) number is K962687.

When did GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM receive FDA 510(k) clearance?

GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM received FDA 510(k) clearance on 1997-03-28, under 510(k) number K962687.

Who is the listed applicant for GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM?

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

What is the FDA product code for GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM?

The FDA product code for GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM is JQW.

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 Nichols Institute Diagnostics 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 68 devices →

Related Devices (Code: JQW)

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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