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)

HEATED INSTRUMENT BATH

K-Number: K870276 · 1987-05-07

ApplicantSimpson/Basye, Inc.
Decision Date1987-05-07
Product CodeLRJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEATED INSTRUMENT BATH is the device name listed in this FDA 510(k) record. The listed applicant is Simpson/Basye, Inc.. It received FDA 510(k) clearance on 1987-05-07 under 510(k) number K870276. The device is classified under product code LRJ. It was reviewed by the HO advisory panel. Product code LRJ falls under the category of Clinical Lab, which includes general clinical laboratory instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEATED INSTRUMENT BATH?

HEATED INSTRUMENT BATH is a medical device that received FDA 510(k) clearance on 1987-05-07. The listed applicant is Simpson/Basye, Inc.. The 510(k) number is K870276.

When did HEATED INSTRUMENT BATH receive FDA 510(k) clearance?

HEATED INSTRUMENT BATH received FDA 510(k) clearance on 1987-05-07, under 510(k) number K870276.

Who is the listed applicant for HEATED INSTRUMENT BATH?

The FDA 510(k) record lists Simpson/Basye, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEATED INSTRUMENT BATH?

The FDA product code for HEATED INSTRUMENT BATH is LRJ. This falls under the Clinical Lab category.

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 Simpson/Basye, Inc. 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.

K926179SEDLACEK HANDLEK891352MARLOW ANAL SPECULUMK891351NEWPORT LATERAL VAGINAL RETRACTORK891349CAMPION CERVICAL HOOKK891350NEWPORT CERVICAL MANIPULATORK891347REID ENDOCERVICAL SPREADER

View all 12 devices →

Related Devices (Code: LRJ)

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.

K992661CONTROL III ELITEMaril Products, Inc.K991509PRO-PORTION CLEANER/DISINFECTANTSultan Chemists, Inc.K984485MICROSTAT 2Chemlink Laboratories, LLCK983947AMERSE 2STERIS CorporationK983869DISPATCH HOSPITAL CLEANER DISINFECTANT TOWELS WITH BLEACHCaltech Industries, Inc.K983585LOW PH PHENOLIC 256Central Solutions, 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.

↑