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FDA 510(k)

ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.

K-Number: K800998 · 1980-05-28

ApplicantGeneral X-Ray, Inc.
Decision Date1980-05-28
Product Code
DecisionSubstantially Equivalent

Device Summary

ATLAS-S X-RAY SYSTEM W/KETROMAT GEN. is the device name listed in this FDA 510(k) record. The listed applicant is General X-Ray, Inc.. It received FDA 510(k) clearance on 1980-05-28 under 510(k) number K800998. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.?

ATLAS-S X-RAY SYSTEM W/KETROMAT GEN. is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is General X-Ray, Inc.. The 510(k) number is K800998.

When did ATLAS-S X-RAY SYSTEM W/KETROMAT GEN. receive FDA 510(k) clearance?

ATLAS-S X-RAY SYSTEM W/KETROMAT GEN. received FDA 510(k) clearance on 1980-05-28, under 510(k) number K800998.

Who is the listed applicant for ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.?

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

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Other records listing General X-Ray, 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.

K790451X-RAY UNITS, GX-101, UCIS-510 AND GX-111K790392510 CARBINETTE X-RAY UNITK790443PORTABLE X-RAY UNITK790393PORTABLE X-RAY UNIT, MATRIX S GX-101K790511MOBILE X-RAY UNITK790512PORTABLE X-RAY UNIT

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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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