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)

STOOL-COLLECTION/PRESERVATION KIT

K-Number: K822870 · 1982-11-01

ApplicantAmerican Scientific Products
Decision Date1982-11-01
Product CodeKDT
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

STOOL-COLLECTION/PRESERVATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Scientific Products. It received FDA 510(k) clearance on 1982-11-01 under 510(k) number K822870. The device is classified under product code KDT. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOOL-COLLECTION/PRESERVATION KIT?

STOOL-COLLECTION/PRESERVATION KIT is a medical device that received FDA 510(k) clearance on 1982-11-01. The listed applicant is American Scientific Products. The 510(k) number is K822870.

When did STOOL-COLLECTION/PRESERVATION KIT receive FDA 510(k) clearance?

STOOL-COLLECTION/PRESERVATION KIT received FDA 510(k) clearance on 1982-11-01, under 510(k) number K822870.

Who is the listed applicant for STOOL-COLLECTION/PRESERVATION KIT?

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

What is the FDA product code for STOOL-COLLECTION/PRESERVATION KIT?

The FDA product code for STOOL-COLLECTION/PRESERVATION KIT is KDT.

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 American Scientific Products 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.

K864824INFECTIOUS TISSUE KITK844042BLOOD DILUTION VIALK831634GLUCOSE REAGENT B6360-11K831625UREA NITROGEN-BUN-REAGENTS B6360-12K831626UREA NITROGEN-BUN-REAGENTS B6370-11AK831628CREATININE REAGENTS B6370-13

View all 28 devices →

Related Devices (Code: KDT)

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.

K873593BIOSURE SPECIMEN COLLECTION CONTAINERBiosure, Inc.K862665NOVACYTE-UXsirius Medical, Inc.K834579BIOSPAL 2400SHospal Medical Corp.K834412PRESERV PVA FIXATIVE 15ML-FORMALIN PKPreventive Diagnostics Corp.K833660PRESERV PVA FIXATIVE -MALIN PACKPreventive Diagnostics Corp.K823773PROVIAL II #006-010-0201Dynatech Corp.

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.

↑