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FDA 510(k)

MANUEL SAFTEY SYRINGE PARTS 1 & 2

K-Number: K060772 · 2006-10-16

ApplicantMedsafe Asa
Decision Date2006-10-16
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MANUEL SAFTEY SYRINGE PARTS 1 & 2 is the device name listed in this FDA 510(k) record. The listed applicant is Medsafe Asa. It received FDA 510(k) clearance on 2006-10-16 under 510(k) number K060772. 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 MANUEL SAFTEY SYRINGE PARTS 1 & 2?

MANUEL SAFTEY SYRINGE PARTS 1 & 2 is a medical device that received FDA 510(k) clearance on 2006-10-16. The listed applicant is Medsafe Asa. The 510(k) number is K060772.

When did MANUEL SAFTEY SYRINGE PARTS 1 & 2 receive FDA 510(k) clearance?

MANUEL SAFTEY SYRINGE PARTS 1 & 2 received FDA 510(k) clearance on 2006-10-16, under 510(k) number K060772.

Who is the listed applicant for MANUEL SAFTEY SYRINGE PARTS 1 & 2?

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

What is the FDA product code for MANUEL SAFTEY SYRINGE PARTS 1 & 2?

The FDA product code for MANUEL SAFTEY SYRINGE PARTS 1 & 2 is MEG.

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: MEG)

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

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

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