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FDA 510(k)

POP-N-LOK SYRINGE

K-Number: K946219 · 1995-12-28

ApplicantRetractable Technologies, Inc.
Decision Date1995-12-28
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POP-N-LOK SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Retractable Technologies, Inc.. It received FDA 510(k) clearance on 1995-12-28 under 510(k) number K946219. 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 POP-N-LOK SYRINGE?

POP-N-LOK SYRINGE is a medical device that received FDA 510(k) clearance on 1995-12-28. The listed applicant is Retractable Technologies, Inc.. The 510(k) number is K946219.

When did POP-N-LOK SYRINGE receive FDA 510(k) clearance?

POP-N-LOK SYRINGE received FDA 510(k) clearance on 1995-12-28, under 510(k) number K946219.

Who is the listed applicant for POP-N-LOK SYRINGE?

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

What is the FDA product code for POP-N-LOK SYRINGE?

The FDA product code for POP-N-LOK SYRINGE is MEG.

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Related Devices (Code: MEG)

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K252098PA3X Detachable Safety Sleeve Syringe (with needle) (SC-23ED / SD-23ED)Methyl Co., Ltd.K250847VaporShieldVault Paragon Group, Inc.K230287SaviSafe Safety DeviceSuzhou Savicred Biotechnology Co., Ltd.K231165Shina Syringe; Shina Safety SyringeShina Med CorporationK231907Medline Safety Insulin and TB SyringesMedline Industries, LPK223376Monoject Magellan Insulin Safety Syringe 1mL, 31G x 6mm (8881893110); Monoject Magellan Insulin Safety Syringe 0.5mL, 31G x 6mm (8881893150); Monoject Magellan Insulin Safety Syringe 0.3mL, 31G x 6mm (8881893130)Cardinal Health200, LLC

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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