510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Inmed Corp.

Mchenry, IL, US

Inmed Corp. appears in FDA device records in Mchenry, IL. FDA records list 24 510(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
24
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 24 510(k) clearances for Inmed Corp. between 1981 and 1984. The busiest year on record is 1984, with 14. The most recent is 1984, with 14.

Clearances by year, as a table
510(k) clearance decisions for Inmed Corp., by decision year
YearClearances
19814
19821
19835
198414
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K842866URETHRAL CATHETERIZATION TRAYKODSubstantially Equivalent
K841040FOX POST NASAL BALLOON CATHETEREMXSubstantially Equivalent
K842865ESOPHAGEAL STETHOSCOPEBZWSubstantially Equivalent
K841037PENROSE DRAINSSubstantially Equivalent
K841039CANTOR TUBEKNTSubstantially Equivalent
K841038BLAKEMORE TUBEKNTSubstantially Equivalent
K841036RECTAL BALLOON CATHETERSKNTSubstantially Equivalent
K841035ULTRA BAKER JEJUNOSTOMY TUBEKNTSubstantially Equivalent
K841034DEAVER T-DRAIN & CATTEL T-DRAINKNTSubstantially Equivalent
K841033MILLER-ABBOTT TUBEKNTSubstantially Equivalent
K840973COLE TUBE-LATEXBTRSubstantially Equivalent
K841093NASOPHARYNGEAL AIRWAYSBTQSubstantially Equivalent
K832363FOLEY CATHETERIZATION TRAY-VARIOUSKODSubstantially Equivalent
K834258HODGE DECOMPRESSION TUBEKNTSubstantially Equivalent
K832859FOAM HELMET - USE W/ESOPHAGEAL TAMPONAKNTSubstantially Equivalent
K832472ELEVATOR CUSHIONFWZSubstantially Equivalent
K832389CATHETER CARE TRAYKODSubstantially Equivalent
K832672FOUR LUMEN BLAKEMORE TUBEKNTSubstantially Equivalent
K832471ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN IIICAESubstantially Equivalent
K820987FOLEY INSERTION TRAYS W/OVERWRAYKODSubstantially Equivalent
K813332BRISTOL BALLON INTRODUCER, MANDRIL SETNWUSubstantially Equivalent
K813169CELESTIN PULSION ESOPHOGEAL PROSTHESISKNTSubstantially Equivalent
K813026GUIDE WIREOCYSubstantially Equivalent
K812289CELESTIN DILATORKNQSubstantially 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

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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