FDA 510(k)

CUP OUT

K-Number: K905027 · 1991-02-05

Decision Date1991-02-05

Product CodeHSZ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

CUP OUT is the device name listed in this FDA 510(k) record. The listed applicant is Anspach Mfg., Inc.. It received FDA 510(k) clearance on 1991-02-05 under 510(k) number K905027. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUP OUT?

CUP OUT is a medical device that received FDA 510(k) clearance on 1991-02-05. The listed applicant is Anspach Mfg., Inc.. The 510(k) number is K905027.

When did CUP OUT receive FDA 510(k) clearance?

CUP OUT received FDA 510(k) clearance on 1991-02-05, under 510(k) number K905027.

Who is the listed applicant for CUP OUT?

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

What is the FDA product code for CUP OUT?

The FDA product code for CUP OUT is HSZ.

Other records listing Anspach Mfg., 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.

K940276FILTER, DIFFUSER K925328ANSPACH BONE RIVET, ANSPACH SUTURE ANCHOR

Related Devices (Code: HSZ)

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical Systems K972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SA K944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, 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.