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FDA 510(k)

VR MEDICAL ENTERAL ORAL SYRINGE

K-Number: K110853 · 2011-05-13

ApplicantVr Medical
Decision Date2011-05-13
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VR MEDICAL ENTERAL ORAL SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Vr Medical. It received FDA 510(k) clearance on 2011-05-13 under 510(k) number K110853. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VR MEDICAL ENTERAL ORAL SYRINGE?

VR MEDICAL ENTERAL ORAL SYRINGE is a medical device that received FDA 510(k) clearance on 2011-05-13. The listed applicant is Vr Medical. The 510(k) number is K110853.

When did VR MEDICAL ENTERAL ORAL SYRINGE receive FDA 510(k) clearance?

VR MEDICAL ENTERAL ORAL SYRINGE received FDA 510(k) clearance on 2011-05-13, under 510(k) number K110853.

Who is the listed applicant for VR MEDICAL ENTERAL ORAL SYRINGE?

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

What is the FDA product code for VR MEDICAL ENTERAL ORAL SYRINGE?

The FDA product code for VR MEDICAL ENTERAL ORAL SYRINGE is FPD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FPD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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