FDA 510(k)

PFF-1

K-Number: K914205 · 1992-05-01

Decision Date1992-05-01

Product CodeBZG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PFF-1 is the device name listed in this FDA 510(k) record. The listed applicant is Cybermedic, Inc.. It received FDA 510(k) clearance on 1992-05-01 under 510(k) number K914205. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFF-1?

PFF-1 is a medical device that received FDA 510(k) clearance on 1992-05-01. The listed applicant is Cybermedic, Inc.. The 510(k) number is K914205.

When did PFF-1 receive FDA 510(k) clearance?

PFF-1 received FDA 510(k) clearance on 1992-05-01, under 510(k) number K914205.

Who is the listed applicant for PFF-1?

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

What is the FDA product code for PFF-1?

The FDA product code for PFF-1 is BZG.

Other records listing Cybermedic, 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.

K941813VENSHIELD K903959NEONATAL METASCOPE K884910MODEL 1010, CY-MET K861418SPINNAKER K851197CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH K842782PHYSIOLOGICAL ANALYZER CM-710

View all 11 devices →

Related Devices (Code: BZG)

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair AB K230501Spirobank OxiMir Medical International Research USA K230178EasyOne Sky SpirometerNdd Medizintechnik AG K222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

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.