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FDA 510(k)

ORTHOVISION TABLE

K-Number: K905816 · 1991-03-06

ApplicantAmerican Sterilizer Co.
Decision Date1991-03-06
Product CodeJEB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORTHOVISION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1991-03-06 under 510(k) number K905816. The device is classified under product code JEB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOVISION TABLE?

ORTHOVISION TABLE is a medical device that received FDA 510(k) clearance on 1991-03-06. The listed applicant is American Sterilizer Co.. The 510(k) number is K905816.

When did ORTHOVISION TABLE receive FDA 510(k) clearance?

ORTHOVISION TABLE received FDA 510(k) clearance on 1991-03-06, under 510(k) number K905816.

Who is the listed applicant for ORTHOVISION TABLE?

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

What is the FDA product code for ORTHOVISION TABLE?

The FDA product code for ORTHOVISION TABLE is JEB.

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Other records listing American Sterilizer Co. 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.

K943288AMSCO SQ240 SURGICAL LIGHTK931872THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZERK922485CHEMDI-VHP CHEMICAL INDICATORK930493QUANTUM 3080 SURGICAL TABLEK896674AMSCO QUANTUM LIGHTK895164EAGLE DS

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Related Devices (Code: JEB)

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.

K900405SCHOLTEN FRAMEScholten Surgical Instruments, Inc.K891917ORTHO-J, INC. BEK-JS-004Ortho-J, Inc.K891387WILLIAMS BELT & BOOTArthro-Medic, Inc.K881101K ORTHOPEDIC TABLEInstrumentation Specialties, Inc.K880263OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSIONOrthopedic Systems, Inc.K873275EXTENSION TABLE 1417Stierlen-Maquet AG

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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