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FDA 510(k)

W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY

K-Number: K944708 · 1995-06-02

ApplicantA-Dec, Inc.
Decision Date1995-06-02
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY is the device name listed in this FDA 510(k) record. The listed applicant is A-Dec, Inc.. It received FDA 510(k) clearance on 1995-06-02 under 510(k) number K944708. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY?

W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY is a medical device that received FDA 510(k) clearance on 1995-06-02. The listed applicant is A-Dec, Inc.. The 510(k) number is K944708.

When did W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY receive FDA 510(k) clearance?

W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY received FDA 510(k) clearance on 1995-06-02, under 510(k) number K944708.

Who is the listed applicant for W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY?

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

What is the FDA product code for W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY?

The FDA product code for W&H 895 TOP LIGH HIGHSPEED FIBEROPTIC SINGLE SPRAY is EFB.

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 A-Dec, 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 68 devices →

Related Devices (Code: EFB)

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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