FDA 510(k)

MODIFIED SERVO SYRINGE

K-Number: K881521 · 1988-05-31

Decision Date1988-05-31

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODIFIED SERVO SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Engineering, Inc.. It received FDA 510(k) clearance on 1988-05-31 under 510(k) number K881521. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED SERVO SYRINGE?

MODIFIED SERVO SYRINGE is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Engineering, Inc.. The 510(k) number is K881521.

When did MODIFIED SERVO SYRINGE receive FDA 510(k) clearance?

MODIFIED SERVO SYRINGE received FDA 510(k) clearance on 1988-05-31, under 510(k) number K881521.

Who is the listed applicant for MODIFIED SERVO SYRINGE?

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

What is the FDA product code for MODIFIED SERVO SYRINGE?

The FDA product code for MODIFIED SERVO SYRINGE is DXT.

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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.