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FDA 510(k)

WATER PIK(R) W/ADD'L CLAIMS

K-Number: K900547 · 1990-06-15

Decision Date1990-06-15
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WATER PIK(R) W/ADD'L CLAIMS is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne Water Pik. It received FDA 510(k) clearance on 1990-06-15 under 510(k) number K900547. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATER PIK(R) W/ADD'L CLAIMS?

WATER PIK(R) W/ADD'L CLAIMS is a medical device that received FDA 510(k) clearance on 1990-06-15. The listed applicant is Teledyne Water Pik. The 510(k) number is K900547.

When did WATER PIK(R) W/ADD'L CLAIMS receive FDA 510(k) clearance?

WATER PIK(R) W/ADD'L CLAIMS received FDA 510(k) clearance on 1990-06-15, under 510(k) number K900547.

Who is the listed applicant for WATER PIK(R) W/ADD'L CLAIMS?

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

What is the FDA product code for WATER PIK(R) W/ADD'L CLAIMS?

The FDA product code for WATER PIK(R) W/ADD'L CLAIMS is EFS.

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 Teledyne Water Pik 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 9 devices →

Related Devices (Code: EFS)

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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