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FDA 510(k)

COUNTWAY SYS. SOILED SPONGES-BLOOD LOS

K-Number: K830273 · 1983-02-28

ApplicantRitmed, Inc.
Decision Date1983-02-28
Product CodeFQA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COUNTWAY SYS. SOILED SPONGES-BLOOD LOS is the device name listed in this FDA 510(k) record. The listed applicant is Ritmed, Inc.. It received FDA 510(k) clearance on 1983-02-28 under 510(k) number K830273. The device is classified under product code FQA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COUNTWAY SYS. SOILED SPONGES-BLOOD LOS?

COUNTWAY SYS. SOILED SPONGES-BLOOD LOS is a medical device that received FDA 510(k) clearance on 1983-02-28. The listed applicant is Ritmed, Inc.. The 510(k) number is K830273.

When did COUNTWAY SYS. SOILED SPONGES-BLOOD LOS receive FDA 510(k) clearance?

COUNTWAY SYS. SOILED SPONGES-BLOOD LOS received FDA 510(k) clearance on 1983-02-28, under 510(k) number K830273.

Who is the listed applicant for COUNTWAY SYS. SOILED SPONGES-BLOOD LOS?

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

What is the FDA product code for COUNTWAY SYS. SOILED SPONGES-BLOOD LOS?

The FDA product code for COUNTWAY SYS. SOILED SPONGES-BLOOD LOS is FQA.

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Other records listing Ritmed, 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.

K833626FLORET FOAM PREP SPONGEK832874ISOVIS WOUND PROTECTORK830270ISOVIS WOUND PROTECTORK830261FLORET STRUNG GAUZE SPONGESK830268FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMINK830266FLORET KITTNER OR K DISSECTOR

View all 22 devices →

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.

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