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FDA 510(k)

SCHULTZ ENDHOLD

K-Number: K833332 · 1983-10-31

ApplicantPolyclinic Medical Center
Decision Date1983-10-31
Product CodeJAY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SCHULTZ ENDHOLD is the device name listed in this FDA 510(k) record. The listed applicant is Polyclinic Medical Center. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K833332. The device is classified under product code JAY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHULTZ ENDHOLD?

SCHULTZ ENDHOLD is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Polyclinic Medical Center. The 510(k) number is K833332.

When did SCHULTZ ENDHOLD receive FDA 510(k) clearance?

SCHULTZ ENDHOLD received FDA 510(k) clearance on 1983-10-31, under 510(k) number K833332.

Who is the listed applicant for SCHULTZ ENDHOLD?

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

What is the FDA product code for SCHULTZ ENDHOLD?

The FDA product code for SCHULTZ ENDHOLD is JAY.

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Other records listing Polyclinic Medical Center 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.

K924935HARD TISSUE REPLACE(HTR(R))-PATIENT-MATCH IMPLANT

Related Devices (Code: JAY)

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.

K944988CUSTOM MEDICAL SUSPENSION STRAPCustom Medical Specialties, Inc.K873491BLOCK, BITE, INTUBATIONB&B Medical Technologies, Inc.K860583DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 1315Dale Medical Products, Inc.K850924JEE FRAME (VENTILATOR CIRCUIT SUPPORT)Vulcan Laboratories, Inc.K850309COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCKAckrad LaboratoriesK840844ENDO-SECUREExidyne, 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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