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)

CABOT MEDICAL IRRIGATION FLUID WARMER SETS

K-Number: K932538 · 1994-02-22

Decision Date1994-02-22
Product CodeLHC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CABOT MEDICAL IRRIGATION FLUID WARMER SETS is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K932538. The device is classified under product code LHC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABOT MEDICAL IRRIGATION FLUID WARMER SETS?

CABOT MEDICAL IRRIGATION FLUID WARMER SETS is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Cabot Medical Corp.. The 510(k) number is K932538.

When did CABOT MEDICAL IRRIGATION FLUID WARMER SETS receive FDA 510(k) clearance?

CABOT MEDICAL IRRIGATION FLUID WARMER SETS received FDA 510(k) clearance on 1994-02-22, under 510(k) number K932538.

Who is the listed applicant for CABOT MEDICAL IRRIGATION FLUID WARMER SETS?

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

What is the FDA product code for CABOT MEDICAL IRRIGATION FLUID WARMER SETS?

The FDA product code for CABOT MEDICAL IRRIGATION FLUID WARMER SETS is LHC.

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.

Other records listing Cabot Medical 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.

View all 38 devices →

Related Devices (Code: LHC)

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.

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.

↑