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FDA 510(k)

SYRINGE TIP CAP

K-Number: K911638 · 1991-06-21

ApplicantConcord/Portex
Decision Date1991-06-21
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYRINGE TIP CAP is the device name listed in this FDA 510(k) record. The listed applicant is Concord/Portex. It received FDA 510(k) clearance on 1991-06-21 under 510(k) number K911638. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYRINGE TIP CAP?

SYRINGE TIP CAP is a medical device that received FDA 510(k) clearance on 1991-06-21. The listed applicant is Concord/Portex. The 510(k) number is K911638.

When did SYRINGE TIP CAP receive FDA 510(k) clearance?

SYRINGE TIP CAP received FDA 510(k) clearance on 1991-06-21, under 510(k) number K911638.

Who is the listed applicant for SYRINGE TIP CAP?

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

What is the FDA product code for SYRINGE TIP CAP?

The FDA product code for SYRINGE TIP CAP is JKA.

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Other records listing Concord/Portex as applicant

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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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