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

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2

K Number: K861890 · Decision Jun 3, 1986
Classifications
1
FEI Numbers
258
Registration Numbers
258
Same Product Code
15
Applicant Total
33
Review Days
18

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2
K Number
K861890
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Richard-Allan Medical Ind., Inc.
Date Received
May 16, 1986
Decision Date
June 3, 1986
Product Code
PPM
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
PPM General Purpose Reagent

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PPM), ordered by most recent decision date.

View all

Other Clearances by Richard-Allan Medical Ind., Inc.

K Number Device Name
K931879 REFLEX HTR
K924200 REFLEX(R) ESC
K926297 REFLEX ESI
K924761 STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD
K900566 RICHARD-ALLAN VESSEL LOOPS
K896262 TITANIUM LIGATING CLIPS
K890314 PROTECTOR (SURGICAL INSTRUMENT)
K873309 REFLEX(TM) CA-T CLIP APPLIER
K862404 REFLEX(TM) CLIP APPLIER
K862223 MICRO THIN* PARAFFIN
Search all 33 clearances from Richard-Allan Medical Ind., Inc. →