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)

AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST

K-Number: K880933 · 1988-07-28

ApplicantAmersham Corp.
Decision Date1988-07-28
Product CodeCEP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST is the device name listed in this FDA 510(k) record. The listed applicant is Amersham Corp.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K880933. The device is classified under product code CEP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST?

AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Amersham Corp.. The 510(k) number is K880933.

When did AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST receive FDA 510(k) clearance?

AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST received FDA 510(k) clearance on 1988-07-28, under 510(k) number K880933.

Who is the listed applicant for AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST?

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

What is the FDA product code for AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST?

The FDA product code for AMERLITE LH-30 ASSAY, LAN.0082/2082 240/144 TEST is CEP.

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 →

Related Devices (Code: CEP)

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.

K013582MAYBE?MOM MINI OVULATION MICROSCOPEMaybe?MomK022829INSTANT-VIEW LH OVULATION PREDICTING TESTAlfa Scientific Designs, Inc.K021409AT HOME OVULATION TEST, MODEL 9032Phamatech, Inc.K013874CLEARPLANE EASY OVULATION TESTUnipath , Ltd.K013323TCI-31 LIFELONG OVULATION TESTERTci New YorkK012252QUIK-CHECK OVULATION PREDICTORACON Laboratories, 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.

↑