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FDA 510(k)

SOLO TIES

K-Number: K930452 · 1993-07-08

ApplicantZulaf, Inc.
Decision Date1993-07-08
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SOLO TIES is the device name listed in this FDA 510(k) record. The listed applicant is Zulaf, Inc.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K930452. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLO TIES?

SOLO TIES is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Zulaf, Inc.. The 510(k) number is K930452.

When did SOLO TIES receive FDA 510(k) clearance?

SOLO TIES received FDA 510(k) clearance on 1993-07-08, under 510(k) number K930452.

Who is the listed applicant for SOLO TIES?

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

What is the FDA product code for SOLO TIES?

The FDA product code for SOLO TIES is EJF.

Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, Inc.

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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