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FDA 510(k)

QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE

K-Number: K931093 · 1994-01-21

Decision Date1994-01-21
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Dentalez Group. It received FDA 510(k) clearance on 1994-01-21 under 510(k) number K931093. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE?

QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Dentalez Group. The 510(k) number is K931093.

When did QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE receive FDA 510(k) clearance?

QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE received FDA 510(k) clearance on 1994-01-21, under 510(k) number K931093.

Who is the listed applicant for QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE?

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

What is the FDA product code for QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE?

The FDA product code for QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE is EIA.

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.

Other records listing Dentalez Group as applicant

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.

View all 13 devices →

Related Devices (Code: EIA)

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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