FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

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K Number: K770795 · Decision Jul 11, 1977
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
11
Review Days
70

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Basic Information

Device Name
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K Number
K770795
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Lukens Corp.
Date Received
May 2, 1977
Decision Date
July 11, 1977
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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Other Clearances by Lukens Corp.

K Number Device Name
K880230 SIXALYZER
K800102 STANFORD STERILE LAP SPONGES
K792471 STANFORD STERILE LAP SPONGES
K791495 LUKENS BONE WAX (GAMMA RADIATION)
K770797 TRAY, CATHETERIZATION W/FOLEY, STERILE
K770799 TRAY, IRRIGATION, STERILE, BASIC
K770796 SKIN SCRUB PREP SET
K770794 SUTURE REMOVAL SET, STERILE
K770798 BLADES, SURGICAL, STERILE
K770800 HANDLES, BLADE, SURGICAL
Search all 11 clearances from Lukens Corp. →