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FDA 510(k)

TARGET PROGRAM & EPSON HX-20 COMPUTER

K-Number: K872877 · 1988-02-12

ApplicantWalter Lorenz Surgical, Inc.
Decision Date1988-02-12
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TARGET PROGRAM & EPSON HX-20 COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Walter Lorenz Surgical, Inc.. It received FDA 510(k) clearance on 1988-02-12 under 510(k) number K872877. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGET PROGRAM & EPSON HX-20 COMPUTER?

TARGET PROGRAM & EPSON HX-20 COMPUTER is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is Walter Lorenz Surgical, Inc.. The 510(k) number is K872877.

When did TARGET PROGRAM & EPSON HX-20 COMPUTER receive FDA 510(k) clearance?

TARGET PROGRAM & EPSON HX-20 COMPUTER received FDA 510(k) clearance on 1988-02-12, under 510(k) number K872877.

Who is the listed applicant for TARGET PROGRAM & EPSON HX-20 COMPUTER?

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

What is the FDA product code for TARGET PROGRAM & EPSON HX-20 COMPUTER?

The FDA product code for TARGET PROGRAM & EPSON HX-20 COMPUTER is HAW.

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Other records listing Walter Lorenz Surgical, Inc. 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.

K063386LORENZ ORTHODONTIC ANCHORAGE SYSTEMK063052LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATESK063506LORENZ STERNAL CLOSURE SYSTEMK062842TWIST DRILLK061384LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUMK042516OTOMIMIX

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Related Devices (Code: HAW)

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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