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FDA 510(k)

MULES SPHERE GLASS (SEVERAL SIZES)

K-Number: K895908 · 1990-01-08

Decision Date1990-01-08
Product CodeHPZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MULES SPHERE GLASS (SEVERAL SIZES) is the device name listed in this FDA 510(k) record. The listed applicant is Ginsberg Scientific, Inc.. It received FDA 510(k) clearance on 1990-01-08 under 510(k) number K895908. The device is classified under product code HPZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULES SPHERE GLASS (SEVERAL SIZES)?

MULES SPHERE GLASS (SEVERAL SIZES) is a medical device that received FDA 510(k) clearance on 1990-01-08. The listed applicant is Ginsberg Scientific, Inc.. The 510(k) number is K895908.

When did MULES SPHERE GLASS (SEVERAL SIZES) receive FDA 510(k) clearance?

MULES SPHERE GLASS (SEVERAL SIZES) received FDA 510(k) clearance on 1990-01-08, under 510(k) number K895908.

Who is the listed applicant for MULES SPHERE GLASS (SEVERAL SIZES)?

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

What is the FDA product code for MULES SPHERE GLASS (SEVERAL SIZES)?

The FDA product code for MULES SPHERE GLASS (SEVERAL SIZES) is HPZ.

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.

Related Devices (Code: HPZ)

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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