Modified X-Ray Table

FDA 510(k) K827582 · Transworld X-Ray Corp.

Substantially Equivalent

510(k) numberK827582

Submission

Device name
Modified X-Ray Table
Applicant
Transworld X-Ray Corp.
Charlotte, NC, US
Received
May 28, 1982
Decision date
July 9, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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Questions and answers

When was Modified X-Ray Table cleared by the FDA?

Modified X-Ray Table (K827582) received a 510(k) decision of Substantially Equivalent on July 9, 1982, 42 days after the submission was received.