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FDA 510(k)

AMSCO ENDOSCOPY TABLE

K-Number: K821749 · 1982-07-09

ApplicantAmerican Sterilizer Co.
Decision Date1982-07-09
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMSCO ENDOSCOPY 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 1982-07-09 under 510(k) number K821749. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSCO ENDOSCOPY TABLE?

AMSCO ENDOSCOPY TABLE is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is American Sterilizer Co.. The 510(k) number is K821749.

When did AMSCO ENDOSCOPY TABLE receive FDA 510(k) clearance?

AMSCO ENDOSCOPY TABLE received FDA 510(k) clearance on 1982-07-09, under 510(k) number K821749.

Who is the listed applicant for AMSCO ENDOSCOPY 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 AMSCO ENDOSCOPY TABLE?

The FDA product code for AMSCO ENDOSCOPY TABLE is GDC.

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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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 TABLEK905816ORTHOVISION TABLEK896674AMSCO QUANTUM LIGHT

View all 36 devices →

Related Devices (Code: GDC)

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.

K971390QUANTUM 3080SP SURGICAL TABLESTERIS CorporationK970807MOBILE OPERATING TABLE 1132.01Stierlen-Maquet AGK964273DURA-BOARD ARMBOARDAllen Medical Systems, Inc.K940616SKYTRON ELITE 3500 TABLESkytron, Div. the Kmw Group, Inc.K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.K914758MDT/SHAMPAINE MODEL 4900B SURGICAL TABLEMdt Corp., 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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