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FDA 510(k)

TRANS-PULSE MODEL #1103

K-Number: K862355 · 1986-08-19

ApplicantThe Sun Co.
Decision Date1986-08-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TRANS-PULSE MODEL #1103 is the device name listed in this FDA 510(k) record. The listed applicant is The Sun Co.. It received FDA 510(k) clearance on 1986-08-19 under 510(k) number K862355. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANS-PULSE MODEL #1103?

TRANS-PULSE MODEL #1103 is a medical device that received FDA 510(k) clearance on 1986-08-19. The listed applicant is The Sun Co.. The 510(k) number is K862355.

When did TRANS-PULSE MODEL #1103 receive FDA 510(k) clearance?

TRANS-PULSE MODEL #1103 received FDA 510(k) clearance on 1986-08-19, under 510(k) number K862355.

Who is the listed applicant for TRANS-PULSE MODEL #1103?

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

What is the FDA product code for TRANS-PULSE MODEL #1103?

The FDA product code for TRANS-PULSE MODEL #1103 is GZJ.

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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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