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

SPENCO CRYOPRESS

K Number: K820906 · Decision May 13, 1982
Classifications
1
FEI Numbers
377
Registration Numbers
377
Same Product Code
81
Applicant Total
10
Review Days
42

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Basic Information

Device Name
SPENCO CRYOPRESS
K Number
K820906
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5710
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Spenco Medical Corp.
Date Received
April 1, 1982
Decision Date
May 13, 1982
Product Code
IMD
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IMD Pack, Hot Or Cold, Disposable

Similar 510(k) Clearances

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

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Other Clearances by Spenco Medical Corp.

K Number Device Name
K981902 SPENCO SILICONE GEL SHEET
K922228 2ND SKIN STERILE ADHESIVE STRIP
K911550 2ND SKIN MOIST BURN PADS WITH ALOE
K910927 SPENCIO SKIN GUARD KIT
K896533 SPENCO BREAST FORMS
K894898 2ND SKIN NON-STICK MOIST BURN PADS
K811184 SPENCO DERMAL PADS
K791726 HYDROGEL-PREP
K791162 GELSKIN