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FDA 510(k)

GNOMOS STEREOTACTIC DEVICE

K-Number: K901670 · 1990-07-03

ApplicantMedical Equipment Development Co., Inc.
Decision Date1990-07-03
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GNOMOS STEREOTACTIC DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Development Co., Inc.. It received FDA 510(k) clearance on 1990-07-03 under 510(k) number K901670. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GNOMOS STEREOTACTIC DEVICE?

GNOMOS STEREOTACTIC DEVICE is a medical device that received FDA 510(k) clearance on 1990-07-03. The listed applicant is Medical Equipment Development Co., Inc.. The 510(k) number is K901670.

When did GNOMOS STEREOTACTIC DEVICE receive FDA 510(k) clearance?

GNOMOS STEREOTACTIC DEVICE received FDA 510(k) clearance on 1990-07-03, under 510(k) number K901670.

Who is the listed applicant for GNOMOS STEREOTACTIC DEVICE?

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

What is the FDA product code for GNOMOS STEREOTACTIC DEVICE?

The FDA product code for GNOMOS STEREOTACTIC DEVICE is HAW.

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Other records listing Medical Equipment Development Co., 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.

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Related Devices (Code: HAW)

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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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