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FDA 510(k)

RETRAX SAFETY SYRINGE

K-Number: K901508 · 1990-06-14

ApplicantRetrax, Inc.
Decision Date1990-06-14
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RETRAX SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Retrax, Inc.. It received FDA 510(k) clearance on 1990-06-14 under 510(k) number K901508. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RETRAX SAFETY SYRINGE?

RETRAX SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 1990-06-14. The listed applicant is Retrax, Inc.. The 510(k) number is K901508.

When did RETRAX SAFETY SYRINGE receive FDA 510(k) clearance?

RETRAX SAFETY SYRINGE received FDA 510(k) clearance on 1990-06-14, under 510(k) number K901508.

Who is the listed applicant for RETRAX SAFETY SYRINGE?

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

What is the FDA product code for RETRAX SAFETY SYRINGE?

The FDA product code for RETRAX SAFETY SYRINGE is FMF.

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Related Devices (Code: FMF)

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.

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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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