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Permeable Technologies, Inc.

Morganville, NJ, US

Permeable Technologies, Inc. appears in FDA device records in Morganville, NJ. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
7
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 7 510(k) clearances for Permeable Technologies, Inc. between 1994 and 1997. The busiest year on record is 1995, with 3. The most recent is 1997, with 1.

Clearances by year, as a table
510(k) clearance decisions for Permeable Technologies, Inc., by decision year
YearClearances
19941
19953
19962
19971
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K963001LIFESTYLE 4-VUE (POLYMACON) HYDROPHILIC MULTIFOCAL CONTACT LENS FOR DAILY WEARLPLSubstantially Equivalent
K963011LIFESTYLE FREQUENCY PROGRESSIVE (METHAFILCON A) MULTIFOCAL HYDROPHILIC CONTACT LENSES FOR DAILY WEARLPLSubstantially Equivalent
K963010LIFESTYLE GP (TELEFOCON B) RIGID GAS PERMEABLE MULTIFOCAL CONTACT LENS FOR DAILY WEARHQDSubstantially Equivalent
K951893LIFESTYLE 55 (OCUFILCON D) HYDROPHILIC CONTACT LENS LIFESTYLE FREQUENCY 55 (OCUFILCON D) GHYDROPHILIC CONTACT LENSLPLSubstantially Equivalent
K950283LIFESTYLE 4-VUE(TM) (POLYMACON) HYDROPHILIC CONTACT LENSLPLSubstantially Equivalent
K945981LIFESTYLE 55 (METHAFILCON A) SOFT HYDROPHILIC CONTACT LENSLPLSubstantially Equivalent
K942494LIFESTYLE MULTIVUE-S (POLYMACON) SOFT HYDROPHILIC CONTACT LENSLPLSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain