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FDA 510(k)

SCANLAN ATRAUM INSTRUMENT JAW COVER

K-Number: K841513 · 1984-07-06

ApplicantScanlan Intl., Inc.
Decision Date1984-07-06
Product Code
DecisionSubstantially Equivalent

Device Summary

SCANLAN ATRAUM INSTRUMENT JAW COVER is the device name listed in this FDA 510(k) record. The listed applicant is Scanlan Intl., Inc.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K841513. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANLAN ATRAUM INSTRUMENT JAW COVER?

SCANLAN ATRAUM INSTRUMENT JAW COVER is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Scanlan Intl., Inc.. The 510(k) number is K841513.

When did SCANLAN ATRAUM INSTRUMENT JAW COVER receive FDA 510(k) clearance?

SCANLAN ATRAUM INSTRUMENT JAW COVER received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841513.

Who is the listed applicant for SCANLAN ATRAUM INSTRUMENT JAW COVER?

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

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Other records listing Scanlan Intl., 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.

K960372SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEMK945474SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDERK911184SCANLAN/TAHERI VALVULOTOMEK864919SCANLAN (TM) VEIN/GRAFT HOLDERK864920SCANLAN (TM) INSTRUMENT TRAYK851825SCANLAN TUNNELER, SHEATH & TIP

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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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