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FDA 510(k)

SURGICAL INSTRUMENT DEMAGNETIZER

K-Number: K841086 · 1984-04-24

ApplicantScanlan Intl., Inc.
Decision Date1984-04-24
Product Code
DecisionSubstantially Equivalent

Device Summary

SURGICAL INSTRUMENT DEMAGNETIZER 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 1984-04-24 under 510(k) number K841086. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL INSTRUMENT DEMAGNETIZER?

SURGICAL INSTRUMENT DEMAGNETIZER is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is Scanlan Intl., Inc.. The 510(k) number is K841086.

When did SURGICAL INSTRUMENT DEMAGNETIZER receive FDA 510(k) clearance?

SURGICAL INSTRUMENT DEMAGNETIZER received FDA 510(k) clearance on 1984-04-24, under 510(k) number K841086.

Who is the listed applicant for SURGICAL INSTRUMENT DEMAGNETIZER?

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 VALVULOTOMEK864920SCANLAN (TM) INSTRUMENT TRAYK864919SCANLAN (TM) VEIN/GRAFT HOLDERK851825SCANLAN TUNNELER, SHEATH & TIP

View all 19 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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