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FDA 510(k)

SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE

K-Number: K882019 · 1988-05-31

Decision Date1988-05-31
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K882019. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE?

SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is General Electric Co.. The 510(k) number is K882019.

When did SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE receive FDA 510(k) clearance?

SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE received FDA 510(k) clearance on 1988-05-31, under 510(k) number K882019.

Who is the listed applicant for SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE?

The FDA product code for SMS 90-15 R&F TABLE AND SMS 14 SPOT FILM DEVICE is IXR.

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 General Electric Co. 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 254 devices →

Related Devices (Code: IXR)

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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