Atlas FDA

IPOS BREAST PROSTHESIS

FDA 510(k) clearance K792372 · decided 1979-12-19

Clearance details

K-number
K792372
Device name
IPOS BREAST PROSTHESIS
Applicant
Ipos KG
Decision
Substantially Equivalent
Date received
1979-11-26
Decision date
1979-12-19
Days to decision
23 days
Clearance type
Traditional
Product code
GBI
Device class
1
Regulation number
878.3800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
FACTOR II PROSTHETIC SILICONE ELASTOMER (K880329)Factor, Ii, Inc.1988-06-01
AHH NATURAL BREAST FORM (K874279)Pacific Prosthetics, Inc.1987-10-29
S.T.A.C.E.M. EXTERNAL BREAST PROSTHESIS MAMMARY (K872714)Roseburg SA1987-07-21
AMOENA BREAST FORMS (K864785)Coloplast Corp.1987-01-08
PERSONALLY(TM), MODEL 241 SIZES 0-12,LEFT & RIGHT (K864786)Coloplast Corp.1987-01-08
AMOENA BREAST FORMS (K853822)Coloplast Corp.1985-09-30
PROSTHESIS OR SURGICAL PADS (K851668)Virginia Hall, Inc.1985-06-04
SILIMED BREAST FORM (K842765)Sil-Med Corp.1984-08-17
CONFORMA (K841559)Beiersdorf, Inc.1984-07-17
TRILICON BREASE PROSTHESIS DIFFERENT (K841171)Baurs Krey Assoc., Inc.1984-04-25
PDM SILOXANE PROSTHETIC ORBIT (K832151)Delaware Prosthetics, Inc.1983-12-19
PDM SILOXANE PROSTHETIC EAR (K832152)Delaware Prosthetics, Inc.1983-12-09

Recalls involving this device

No recalls on record reference this clearance.