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FDA 510(k)

SONI-LOK SCOPE STABILIZER

K-Number: K850122 · 1985-02-21

ApplicantMed Surg Designs, Inc.
Decision Date1985-02-21
Product CodeFXR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SONI-LOK SCOPE STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Med Surg Designs, Inc.. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K850122. The device is classified under product code FXR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONI-LOK SCOPE STABILIZER?

SONI-LOK SCOPE STABILIZER is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is Med Surg Designs, Inc.. The 510(k) number is K850122.

When did SONI-LOK SCOPE STABILIZER receive FDA 510(k) clearance?

SONI-LOK SCOPE STABILIZER received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850122.

Who is the listed applicant for SONI-LOK SCOPE STABILIZER?

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

What is the FDA product code for SONI-LOK SCOPE STABILIZER?

The FDA product code for SONI-LOK SCOPE STABILIZER is FXR.

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Other records listing Med Surg Designs, Inc. as applicant

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Related Devices (Code: FXR)

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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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