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FDA 510(k)

SPECT TABLE, MODEL #056-760

K-Number: K915541 · 1992-01-17

Decision Date1992-01-17
Product CodeIYZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPECT TABLE, MODEL #056-760 is the device name listed in this FDA 510(k) record. The listed applicant is Atomic Products Corp.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K915541. The device is classified under product code IYZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECT TABLE, MODEL #056-760?

SPECT TABLE, MODEL #056-760 is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Atomic Products Corp.. The 510(k) number is K915541.

When did SPECT TABLE, MODEL #056-760 receive FDA 510(k) clearance?

SPECT TABLE, MODEL #056-760 received FDA 510(k) clearance on 1992-01-17, under 510(k) number K915541.

Who is the listed applicant for SPECT TABLE, MODEL #056-760?

The FDA 510(k) record lists Atomic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECT TABLE, MODEL #056-760?

The FDA product code for SPECT TABLE, MODEL #056-760 is IYZ.

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 Atomic Products Corp. 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: IYZ)

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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