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FDA 510(k)

PRESSURE SENSING SYRINGE 65000

K-Number: K853586 · 1985-11-14

ApplicantDlp, Inc.
Decision Date1985-11-14
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PRESSURE SENSING SYRINGE 65000 is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1985-11-14 under 510(k) number K853586. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE SENSING SYRINGE 65000?

PRESSURE SENSING SYRINGE 65000 is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is Dlp, Inc.. The 510(k) number is K853586.

When did PRESSURE SENSING SYRINGE 65000 receive FDA 510(k) clearance?

PRESSURE SENSING SYRINGE 65000 received FDA 510(k) clearance on 1985-11-14, under 510(k) number K853586.

Who is the listed applicant for PRESSURE SENSING SYRINGE 65000?

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

What is the FDA product code for PRESSURE SENSING SYRINGE 65000?

The FDA product code for PRESSURE SENSING SYRINGE 65000 is DTL.

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Related Devices (Code: DTL)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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