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FDA 510(k)

VIBRA-SURGE SYSTEM MODEL VS2120

K-Number: K971533 · 1997-07-25

ApplicantSonics & Materials, Inc.
Decision Date1997-07-25
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

VIBRA-SURGE SYSTEM MODEL VS2120 is the device name listed in this FDA 510(k) record. The listed applicant is Sonics & Materials, Inc.. It received FDA 510(k) clearance on 1997-07-25 under 510(k) number K971533. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBRA-SURGE SYSTEM MODEL VS2120?

VIBRA-SURGE SYSTEM MODEL VS2120 is a medical device that received FDA 510(k) clearance on 1997-07-25. The listed applicant is Sonics & Materials, Inc.. The 510(k) number is K971533.

When did VIBRA-SURGE SYSTEM MODEL VS2120 receive FDA 510(k) clearance?

VIBRA-SURGE SYSTEM MODEL VS2120 received FDA 510(k) clearance on 1997-07-25, under 510(k) number K971533.

Who is the listed applicant for VIBRA-SURGE SYSTEM MODEL VS2120?

The FDA 510(k) record lists Sonics & Materials, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIBRA-SURGE SYSTEM MODEL VS2120?

The FDA product code for VIBRA-SURGE SYSTEM MODEL VS2120 is LFL.

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Related Devices (Code: LFL)

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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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