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FDA 510(k)

CURITY PLASTIC LOSS OF RESISTANCE SYRINGE

K-Number: K922162 · 1993-04-07

Decision Date1993-04-07
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY PLASTIC LOSS OF RESISTANCE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1993-04-07 under 510(k) number K922162. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY PLASTIC LOSS OF RESISTANCE SYRINGE?

CURITY PLASTIC LOSS OF RESISTANCE SYRINGE is a medical device that received FDA 510(k) clearance on 1993-04-07. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K922162.

When did CURITY PLASTIC LOSS OF RESISTANCE SYRINGE receive FDA 510(k) clearance?

CURITY PLASTIC LOSS OF RESISTANCE SYRINGE received FDA 510(k) clearance on 1993-04-07, under 510(k) number K922162.

Who is the listed applicant for CURITY PLASTIC LOSS OF RESISTANCE SYRINGE?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURITY PLASTIC LOSS OF RESISTANCE SYRINGE?

The FDA product code for CURITY PLASTIC LOSS OF RESISTANCE SYRINGE is CAZ.

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 Kendall Healthcare Products Co. Div.Of Tyco Health 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 66 devices →

Related Devices (Code: CAZ)

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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