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FDA 510(k)

CYTOSTATIC FILTRATION SET

K-Number: K863218 · 1987-02-12

ApplicantMeadox Surgimed, Inc.
Decision Date1987-02-12
Product CodeLFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CYTOSTATIC FILTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Meadox Surgimed, Inc.. It received FDA 510(k) clearance on 1987-02-12 under 510(k) number K863218. The device is classified under product code LFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYTOSTATIC FILTRATION SET?

CYTOSTATIC FILTRATION SET is a medical device that received FDA 510(k) clearance on 1987-02-12. The listed applicant is Meadox Surgimed, Inc.. The 510(k) number is K863218.

When did CYTOSTATIC FILTRATION SET receive FDA 510(k) clearance?

CYTOSTATIC FILTRATION SET received FDA 510(k) clearance on 1987-02-12, under 510(k) number K863218.

Who is the listed applicant for CYTOSTATIC FILTRATION SET?

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

What is the FDA product code for CYTOSTATIC FILTRATION SET?

The FDA product code for CYTOSTATIC FILTRATION SET is LFK.

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Other records listing Meadox Surgimed, 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.

K944143MS CLASSIQUE BALLOON CATHETERK945061NOPROFILE OLBERT CATHETER SYSTEMK942382MS AMPLATZ EXTRA STIFF GUIDE WIREK930201ACECUT SUTOMATIC BIOPSY SYSTEMK911635MEADOX(R) SURGIMED(R) BIOPSY GUN IIK905181NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGY

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Related Devices (Code: LFK)

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.

K971897CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH)Medron, Inc.K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETAkcess Medical Products, Inc.K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSAkcess Medical Products, Inc.K891763FC-100 FEMORAL CATHETERAkcess Medical Products, Inc.K891764FC-101 FEMORAL CATHETER GUIDE WIREAkcess Medical Products, Inc.K890717MODIFICATION HEMOFILTRATION CATHETER HF-100Vas-Cath, 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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