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FDA 510(k)

ULTIMAT L4 X L4, LIEBEL-FLARSHEIM

K-Number: K770836 · 1977-05-26

ApplicantMallinckrodt Group, Inc.
Decision Date1977-05-26
Product CodeKPX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTIMAT L4 X L4, LIEBEL-FLARSHEIM is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1977-05-26 under 510(k) number K770836. The device is classified under product code KPX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIMAT L4 X L4, LIEBEL-FLARSHEIM?

ULTIMAT L4 X L4, LIEBEL-FLARSHEIM is a medical device that received FDA 510(k) clearance on 1977-05-26. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K770836.

When did ULTIMAT L4 X L4, LIEBEL-FLARSHEIM receive FDA 510(k) clearance?

ULTIMAT L4 X L4, LIEBEL-FLARSHEIM received FDA 510(k) clearance on 1977-05-26, under 510(k) number K770836.

Who is the listed applicant for ULTIMAT L4 X L4, LIEBEL-FLARSHEIM?

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

What is the FDA product code for ULTIMAT L4 X L4, LIEBEL-FLARSHEIM?

The FDA product code for ULTIMAT L4 X L4, LIEBEL-FLARSHEIM is KPX.

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Other records listing Mallinckrodt Group, Inc. as applicant

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Related Devices (Code: KPX)

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.

K945635TRANS X-1000Canon USA, Inc.K935157ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBESRegulatory Consultants TO the Medical Device IndusK934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSVictoreen, Inc.K933035BCM-600TXB C Medical , Ltd.K925598BUCKYMATIC AUTOMATIC CHEST FILM CHANGERAcoma Medical Imaging, Inc.K924423MWX-7440 HIGH SPEED BUCKYMidwest X-Ray Equipment Co.

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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