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)

MONITOR, RADIOISOTOPE, MODEL 9273A

K-Number: K770397 · 1977-03-10

ApplicantAmersham Corp.
Decision Date1977-03-10
Product Code
DecisionSubstantially Equivalent

Device Summary

MONITOR, RADIOISOTOPE, MODEL 9273A is the device name listed in this FDA 510(k) record. The listed applicant is Amersham Corp.. It received FDA 510(k) clearance on 1977-03-10 under 510(k) number K770397. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR, RADIOISOTOPE, MODEL 9273A?

MONITOR, RADIOISOTOPE, MODEL 9273A is a medical device that received FDA 510(k) clearance on 1977-03-10. The listed applicant is Amersham Corp.. The 510(k) number is K770397.

When did MONITOR, RADIOISOTOPE, MODEL 9273A receive FDA 510(k) clearance?

MONITOR, RADIOISOTOPE, MODEL 9273A received FDA 510(k) clearance on 1977-03-10, under 510(k) number K770397.

Who is the listed applicant for MONITOR, RADIOISOTOPE, MODEL 9273A?

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

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 Amersham Corp. 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.

K914135AMERLITE(TM) PROLACTIN-30 ASSAY, LAN.0086/2086K912733AMERLEX-M SPECIFIC ESTROL(UNCONJUGATED) RIA KITK912766AMERLITE CK-MB ASSAYK904666AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008K902760AMERSHAM TSH CONTROL SERAK901832GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415

View all 94 devices →

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.

↑