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FDA 510(k)

MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002

K-Number: K903018 · 1990-12-03

ApplicantMedtronic Andover Medical, Inc.
Decision Date1990-12-03
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Andover Medical, Inc.. It received FDA 510(k) clearance on 1990-12-03 under 510(k) number K903018. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002?

MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 is a medical device that received FDA 510(k) clearance on 1990-12-03. The listed applicant is Medtronic Andover Medical, Inc.. The 510(k) number is K903018.

When did MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 receive FDA 510(k) clearance?

MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 received FDA 510(k) clearance on 1990-12-03, under 510(k) number K903018.

Who is the listed applicant for MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002?

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

What is the FDA product code for MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002?

The FDA product code for MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002 is LDD.

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Other records listing Medtronic Andover Medical, 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.

K910494RESTING EKG ELECTRODE SERIESK905446MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODEK903554NORTECH MODEL 87202204 ELECTRODEK882174MODIFIED MODEL 5455 DISPOSABLE SURGICAL CABLEK852469SAF-D-FIB

Related Devices (Code: LDD)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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