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FDA 510(k)

LAPARETTE

K-Number: K971146 · 1997-08-25

ApplicantRd Chus, Inc.
Decision Date1997-08-25
Product CodeKNF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPARETTE is the device name listed in this FDA 510(k) record. The listed applicant is Rd Chus, Inc.. It received FDA 510(k) clearance on 1997-08-25 under 510(k) number K971146. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPARETTE?

LAPARETTE is a medical device that received FDA 510(k) clearance on 1997-08-25. The listed applicant is Rd Chus, Inc.. The 510(k) number is K971146.

When did LAPARETTE receive FDA 510(k) clearance?

LAPARETTE received FDA 510(k) clearance on 1997-08-25, under 510(k) number K971146.

Who is the listed applicant for LAPARETTE?

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

What is the FDA product code for LAPARETTE?

The FDA product code for LAPARETTE is KNF.

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Related Devices (Code: KNF)

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

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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