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FDA 510(k)

SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES

K-Number: K874681 · 1988-02-05

ApplicantKlockner Contract Packaging, Inc.
Decision Date1988-02-05
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES is the device name listed in this FDA 510(k) record. The listed applicant is Klockner Contract Packaging, Inc.. It received FDA 510(k) clearance on 1988-02-05 under 510(k) number K874681. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES?

SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is Klockner Contract Packaging, Inc.. The 510(k) number is K874681.

When did SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES receive FDA 510(k) clearance?

SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES received FDA 510(k) clearance on 1988-02-05, under 510(k) number K874681.

Who is the listed applicant for SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES?

The FDA 510(k) record lists Klockner Contract Packaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES?

The FDA product code for SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES is HQG.

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Related Devices (Code: HQG)

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.

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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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