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)

STAIN, HEMASTAIN RETIC

K-Number: K790042 · 1979-02-15

ApplicantGeometric Data, Div. Smithkline Corp.
Decision Date1979-02-15
Product CodeGJH
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STAIN, HEMASTAIN RETIC is the device name listed in this FDA 510(k) record. The listed applicant is Geometric Data, Div. Smithkline Corp.. It received FDA 510(k) clearance on 1979-02-15 under 510(k) number K790042. The device is classified under product code GJH. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAIN, HEMASTAIN RETIC?

STAIN, HEMASTAIN RETIC is a medical device that received FDA 510(k) clearance on 1979-02-15. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K790042.

When did STAIN, HEMASTAIN RETIC receive FDA 510(k) clearance?

STAIN, HEMASTAIN RETIC received FDA 510(k) clearance on 1979-02-15, under 510(k) number K790042.

Who is the listed applicant for STAIN, HEMASTAIN RETIC?

The FDA 510(k) record lists Geometric Data, Div. Smithkline Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAIN, HEMASTAIN RETIC?

The FDA product code for STAIN, HEMASTAIN RETIC is GJH.

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 Geometric Data, Div. Smithkline 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.

K841852AUTOLYZER 800K811534HEMASPINNERK791041HEMATRAK ABNORMAL RECOGNITIONK791108CONTEXT FILTERK790816HEMATRAK MODEL 480K780577PLATELETS/CU MM

View all 18 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.

↑