FDA 510(k)

VACUUM SURGE SUPRESSER

K-Number: K950600 · 1995-05-10

ApplicantSurgin Surgical Instrumentation, Inc.

Decision Date1995-05-10

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

VACUUM SURGE SUPRESSER is the device name listed in this FDA 510(k) record. The listed applicant is Surgin Surgical Instrumentation, Inc.. It received FDA 510(k) clearance on 1995-05-10 under 510(k) number K950600. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM SURGE SUPRESSER?

VACUUM SURGE SUPRESSER is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is Surgin Surgical Instrumentation, Inc.. The 510(k) number is K950600.

When did VACUUM SURGE SUPRESSER receive FDA 510(k) clearance?

VACUUM SURGE SUPRESSER received FDA 510(k) clearance on 1995-05-10, under 510(k) number K950600.

Who is the listed applicant for VACUUM SURGE SUPRESSER?

The FDA 510(k) record lists Surgin Surgical Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUUM SURGE SUPRESSER?

The FDA product code for VACUUM SURGE SUPRESSER is HQC.

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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.