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)

HEATING BLOCK, WAMPOLE 37 C

K-Number: K790549 · 1979-05-03

ApplicantArmkel, LLC
Decision Date1979-05-03
Product CodeJRG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HEATING BLOCK, WAMPOLE 37 C is the device name listed in this FDA 510(k) record. The listed applicant is Armkel, LLC. It received FDA 510(k) clearance on 1979-05-03 under 510(k) number K790549. The device is classified under product code JRG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEATING BLOCK, WAMPOLE 37 C?

HEATING BLOCK, WAMPOLE 37 C is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Armkel, LLC. The 510(k) number is K790549.

When did HEATING BLOCK, WAMPOLE 37 C receive FDA 510(k) clearance?

HEATING BLOCK, WAMPOLE 37 C received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790549.

Who is the listed applicant for HEATING BLOCK, WAMPOLE 37 C?

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

What is the FDA product code for HEATING BLOCK, WAMPOLE 37 C?

The FDA product code for HEATING BLOCK, WAMPOLE 37 C is JRG.

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 Armkel, LLC 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.

K040866FIRST RESPONSE ONE-STEP DIGITAL PREGNANCY TESTK030258FIRST RESPONSE PREGNANCY TESTK023405TROJAN MINT TINGLE BRAND LATEX CONDOMSK013433TROJAN PASSION BERRY GELK013614TROJAN CRYSTAL CLEAR LIQUIDK001212TROJAN EXTRA LARGE LATEX CONDOM

View all 68 devices →

Related Devices (Code: JRG)

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.

K823766BLOOD GAS INCUBATOR #260650Boekel Industries, Inc.K781501ENZAC INCUBATORBd Becton Dickinson Vacutainer Systems Preanalytic

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.

↑