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FDA 510(k)

ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE

K-Number: K983678 · 1999-01-15

ApplicantElekta Instruments, Inc.
Decision Date1999-01-15
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Elekta Instruments, Inc.. It received FDA 510(k) clearance on 1999-01-15 under 510(k) number K983678. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE?

ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE is a medical device that received FDA 510(k) clearance on 1999-01-15. The listed applicant is Elekta Instruments, Inc.. The 510(k) number is K983678.

When did ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE receive FDA 510(k) clearance?

ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE received FDA 510(k) clearance on 1999-01-15, under 510(k) number K983678.

Who is the listed applicant for ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE?

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

What is the FDA product code for ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE?

The FDA product code for ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE is JAI.

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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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