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)

HISTOCHEMICAL PAS REACTION SET

K-Number: K760031 · 1976-07-20

ApplicantHarleco
Decision Date1976-07-20
Product CodeHZT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HISTOCHEMICAL PAS REACTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Harleco. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760031. The device is classified under product code HZT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HISTOCHEMICAL PAS REACTION SET?

HISTOCHEMICAL PAS REACTION SET is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Harleco. The 510(k) number is K760031.

When did HISTOCHEMICAL PAS REACTION SET receive FDA 510(k) clearance?

HISTOCHEMICAL PAS REACTION SET received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760031.

Who is the listed applicant for HISTOCHEMICAL PAS REACTION SET?

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

What is the FDA product code for HISTOCHEMICAL PAS REACTION SET?

The FDA product code for HISTOCHEMICAL PAS REACTION SET is HZT.

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 Harleco 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.

K820233ULTRAZYME PLUS GAMMA GT(65055-65056)K813427ULTRACHEM GLUC-DHK813038ULTRACHEM TP, ITEM #64974K813041ULTRAZYME-GT, ITEM #64959 & 65032K813042ULTRACHEM GLUC-DH SET, ITEM #65048K813044ULTRACHEM ALB, ITEM #64970

View all 116 devices →

Related Devices (Code: HZT)

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.

K883217SCHIFF REAGENTSurgipath Medical Industries, Inc.K843752SIGMA PERIODIC ACID-SCHIFF STAIN 395Sigma Chemical Co.K842919SCHIFF REAGENT FUCHSIN-SULFUROUS ACIDE K Ind., Inc.K842917SCHIFF REAGENT, PAS STAINE K Ind., 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.

↑