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FDA 510(k)

BD SPRING BASED SYRINGE

K-Number: K011103 · 2001-06-13

ApplicantBd
Decision Date2001-06-13
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD SPRING BASED SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Bd. It received FDA 510(k) clearance on 2001-06-13 under 510(k) number K011103. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD SPRING BASED SYRINGE?

BD SPRING BASED SYRINGE is a medical device that received FDA 510(k) clearance on 2001-06-13. The listed applicant is Bd. The 510(k) number is K011103.

When did BD SPRING BASED SYRINGE receive FDA 510(k) clearance?

BD SPRING BASED SYRINGE received FDA 510(k) clearance on 2001-06-13, under 510(k) number K011103.

Who is the listed applicant for BD SPRING BASED SYRINGE?

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

What is the FDA product code for BD SPRING BASED SYRINGE?

The FDA product code for BD SPRING BASED SYRINGE is MEG.

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Related Devices (Code: MEG)

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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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