Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TABLE, EXAMINING-TWO EIGHTY

K-Number: K782064 · 1978-12-28

ApplicantAmsco Co.
Decision Date1978-12-28
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TABLE, EXAMINING-TWO EIGHTY is the device name listed in this FDA 510(k) record. The listed applicant is Amsco Co.. It received FDA 510(k) clearance on 1978-12-28 under 510(k) number K782064. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE, EXAMINING-TWO EIGHTY?

TABLE, EXAMINING-TWO EIGHTY is a medical device that received FDA 510(k) clearance on 1978-12-28. The listed applicant is Amsco Co.. The 510(k) number is K782064.

When did TABLE, EXAMINING-TWO EIGHTY receive FDA 510(k) clearance?

TABLE, EXAMINING-TWO EIGHTY received FDA 510(k) clearance on 1978-12-28, under 510(k) number K782064.

Who is the listed applicant for TABLE, EXAMINING-TWO EIGHTY?

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

What is the FDA product code for TABLE, EXAMINING-TWO EIGHTY?

The FDA product code for TABLE, EXAMINING-TWO EIGHTY is ETF.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Amsco 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.

K912471EAGLE 3000 SDSK854922AMSCO POLARIS SLK833187HALL OSTEONK832945EAGLE 2000 STERILIZER SERIES GAS/AERAK832186HALL DRILL/REAMERK832187HALL OSCILLATOR

View all 19 devices →

Related Devices (Code: ETF)

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.

K953457JEDMED SPECTRUM ENT CABINETJedmed Instrument Co.K945395PREMIER MIRROR WARMERPremier Dental Products Co.K932470LANGGASSE 90Happersberger Otopront GmbHK911901MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCEStortzK910781#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCESMidmark Corp.K910243MOBILE TREATMENT CARTJedmed Instrument Co.

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.

↑