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FDA 510(k)

TIP TOP(R) DISPENSER CAPS

K-Number: K896670 · 1990-03-23

Decision Date1990-03-23
Product CodeGJW
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TIP TOP(R) DISPENSER CAPS is the device name listed in this FDA 510(k) record. The listed applicant is Helena Laboratories. It received FDA 510(k) clearance on 1990-03-23 under 510(k) number K896670. The device is classified under product code GJW. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIP TOP(R) DISPENSER CAPS?

TIP TOP(R) DISPENSER CAPS is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is Helena Laboratories. The 510(k) number is K896670.

When did TIP TOP(R) DISPENSER CAPS receive FDA 510(k) clearance?

TIP TOP(R) DISPENSER CAPS received FDA 510(k) clearance on 1990-03-23, under 510(k) number K896670.

Who is the listed applicant for TIP TOP(R) DISPENSER CAPS?

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

What is the FDA product code for TIP TOP(R) DISPENSER CAPS?

The FDA product code for TIP TOP(R) DISPENSER CAPS is GJW.

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 Helena Laboratories 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 280 devices →

Related Devices (Code: GJW)

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

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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