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FDA 510(k)

ELLIPSE PUNCH

K-Number: K904869 · 1991-03-06

ApplicantKramer Const
Decision Date1991-03-06
Product CodeLRY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELLIPSE PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Kramer Const. It received FDA 510(k) clearance on 1991-03-06 under 510(k) number K904869. The device is classified under product code LRY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELLIPSE PUNCH?

ELLIPSE PUNCH is a medical device that received FDA 510(k) clearance on 1991-03-06. The listed applicant is Kramer Const. The 510(k) number is K904869.

When did ELLIPSE PUNCH receive FDA 510(k) clearance?

ELLIPSE PUNCH received FDA 510(k) clearance on 1991-03-06, under 510(k) number K904869.

Who is the listed applicant for ELLIPSE PUNCH?

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

What is the FDA product code for ELLIPSE PUNCH?

The FDA product code for ELLIPSE PUNCH is LRY.

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.

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Related Devices (Code: LRY)

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.

K933516ACU-E PUNCHAcuderm, Inc.K902636LIPOGEN RHEUMELISA DSDNA ASSAYLipogen, Inc.K896303BIOPSY PUNCHPremier MedicalK874356PIN PUNCHMed-Tool, Inc.K874357TAPERED PUNCHMed-Tool, Inc.K872388NAIL SETMed-Tool, Inc.

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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