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FDA 510(k)

HELLER TRANSILLUMINATING STYLETTE

K-Number: K925061 · 1994-06-27

ApplicantDevice Resources
Decision Date1994-06-27
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HELLER TRANSILLUMINATING STYLETTE is the device name listed in this FDA 510(k) record. The listed applicant is Device Resources. It received FDA 510(k) clearance on 1994-06-27 under 510(k) number K925061. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HELLER TRANSILLUMINATING STYLETTE?

HELLER TRANSILLUMINATING STYLETTE is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Device Resources. The 510(k) number is K925061.

When did HELLER TRANSILLUMINATING STYLETTE receive FDA 510(k) clearance?

HELLER TRANSILLUMINATING STYLETTE received FDA 510(k) clearance on 1994-06-27, under 510(k) number K925061.

Who is the listed applicant for HELLER TRANSILLUMINATING STYLETTE?

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

What is the FDA product code for HELLER TRANSILLUMINATING STYLETTE?

The FDA product code for HELLER TRANSILLUMINATING STYLETTE is KNT.

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Related Devices (Code: KNT)

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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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