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FDA 510(k)

LINE CADDY

K-Number: K810294 · 1981-02-26

ApplicantInstranetics, Inc.
Decision Date1981-02-26
Product CodeHXB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LINE CADDY is the device name listed in this FDA 510(k) record. The listed applicant is Instranetics, Inc.. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810294. The device is classified under product code HXB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINE CADDY?

LINE CADDY is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is Instranetics, Inc.. The 510(k) number is K810294.

When did LINE CADDY receive FDA 510(k) clearance?

LINE CADDY received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810294.

Who is the listed applicant for LINE CADDY?

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

What is the FDA product code for LINE CADDY?

The FDA product code for LINE CADDY is HXB.

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Other records listing Instranetics, 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.

K823430INSTRA-SAFEK811824CAUTERY CADDY PADK811822TIP-VUK811823SHARPS CADDY FBK810208BLADE SAFEK802865SAFE T COUNT

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Related Devices (Code: HXB)

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.

K960539DIAO HAND SURGERY SETKinetikos Medical, Inc.K943472COHORT AVB RETRACTOR SYSTEMCohort Medical Products Group, Inc.K912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedicsK890227SURGICAL PROBEKinetic Medical ProductsK873651BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375Arthropedics, Inc.K873652HOOK PROBE #TM-1376Arthropedics, Inc.

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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