Atlas FDA

THE EMMETT IUD THREAD RETRIEVER

FDA 510(k) clearance K811761 · decided 1981-09-21

Clearance details

K-number
K811761
Device name
THE EMMETT IUD THREAD RETRIEVER
Applicant
Proto-Med, Inc.
Decision
Substantially Equivalent
Date received
1981-06-22
Decision date
1981-09-21
Days to decision
91 days
Clearance type
Traditional
Product code
HHF
Device class
1
Regulation number
884.4530
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
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
IUD HOOKS (K926541)Thomasville Medical Assoc.1994-02-24
IUD HOOKS - SIMPLE, UNIVERSAL AND SKLAR (K891030)Zinnanti Surgical Instruments, Inc.1989-03-17
INTRAUTERINE DEVICE REMOVER (K842295)Premier Dental Products Co.1984-10-12
RELIANCE TEMPO OPHTH. INSTR STAND (K831568)F. & F. Koenigkramer1983-06-30
EMMETT IUD THREAD RETREIVER (K820115)Proto-Med, Inc.1982-02-05

Recalls involving this device

No recalls on record reference this clearance.