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FDA 510(k)

SURGI STIM

K-Number: K982388 · 1998-09-14

ApplicantVision Quest Industries, Inc.
Decision Date1998-09-14
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SURGI STIM is the device name listed in this FDA 510(k) record. The listed applicant is Vision Quest Industries, Inc.. It received FDA 510(k) clearance on 1998-09-14 under 510(k) number K982388. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGI STIM?

SURGI STIM is a medical device that received FDA 510(k) clearance on 1998-09-14. The listed applicant is Vision Quest Industries, Inc.. The 510(k) number is K982388.

When did SURGI STIM receive FDA 510(k) clearance?

SURGI STIM received FDA 510(k) clearance on 1998-09-14, under 510(k) number K982388.

Who is the listed applicant for SURGI STIM?

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

What is the FDA product code for SURGI STIM?

The FDA product code for SURGI STIM is IPF.

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Other records listing Vision Quest Industries, Inc. 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.

K090532T.E.A.R. TECH3K072799TARGET STERILE ELECTRODEK041092FAST START TENS, MODEL FS 3001K030507T.E.A.R. TECH3 MODEL #44TT03

Related Devices (Code: IPF)

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.

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Official Source

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