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FDA 510(k)

SECURET DRAPE & INSTRUMENT RETAINER/INCL

K-Number: K830276 · 1983-03-29

ApplicantRitmed, Inc.
Decision Date1983-03-29
Product CodeGTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SECURET DRAPE & INSTRUMENT RETAINER/INCL is the device name listed in this FDA 510(k) record. The listed applicant is Ritmed, Inc.. It received FDA 510(k) clearance on 1983-03-29 under 510(k) number K830276. The device is classified under product code GTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECURET DRAPE & INSTRUMENT RETAINER/INCL?

SECURET DRAPE & INSTRUMENT RETAINER/INCL is a medical device that received FDA 510(k) clearance on 1983-03-29. The listed applicant is Ritmed, Inc.. The 510(k) number is K830276.

When did SECURET DRAPE & INSTRUMENT RETAINER/INCL receive FDA 510(k) clearance?

SECURET DRAPE & INSTRUMENT RETAINER/INCL received FDA 510(k) clearance on 1983-03-29, under 510(k) number K830276.

Who is the listed applicant for SECURET DRAPE & INSTRUMENT RETAINER/INCL?

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 SECURET DRAPE & INSTRUMENT RETAINER/INCL?

The FDA product code for SECURET DRAPE & INSTRUMENT RETAINER/INCL is GTC.

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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

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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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