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FDA 510(k)

CRAFON ARTHROSCOPY LINES

K-Number: K830673 · 1983-06-08

ApplicantGambro, Inc.
Decision Date1983-06-08
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CRAFON ARTHROSCOPY LINES is the device name listed in this FDA 510(k) record. The listed applicant is Gambro, Inc.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K830673. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRAFON ARTHROSCOPY LINES?

CRAFON ARTHROSCOPY LINES is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Gambro, Inc.. The 510(k) number is K830673.

When did CRAFON ARTHROSCOPY LINES receive FDA 510(k) clearance?

CRAFON ARTHROSCOPY LINES received FDA 510(k) clearance on 1983-06-08, under 510(k) number K830673.

Who is the listed applicant for CRAFON ARTHROSCOPY LINES?

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

What is the FDA product code for CRAFON ARTHROSCOPY LINES?

The FDA product code for CRAFON ARTHROSCOPY LINES is HRX.

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Other records listing Gambro, Inc. as applicant

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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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