Atlas FDA

TYMPANOPLASTY & SKIN DISSECTORS

FDA 510(k) clearance K822569 · decided 1982-10-06

Clearance details

K-number
K822569
Device name
TYMPANOPLASTY & SKIN DISSECTORS
Applicant
Kelleher Corp.
Decision
Substantially Equivalent
Date received
1982-08-24
Decision date
1982-10-06
Days to decision
43 days
Clearance type
Traditional
Product code
GDI
Device class
1
Regulation number
878.4800
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
DISPOSABLE EXTERNAL CLAMPS (K896383)Galenica Enterprises, Inc.1989-12-06
HEPATIC PARENCHYMAL SUCTION DISSECTOR (K850288)Beecher Medical Diagnostic Instrumentation1985-03-18
ROUND-BEEHIVE- DISSECTORS 3/8 (K831912)Ormed Mfg., Inc.1983-10-31
FIELD SUCTION DISSECTOR (K803292)V. Mueller O.V. Baxter Healthcare Corp.1981-01-29
DISPOSABLE SPECIALITY SPONGES (K791870)Carwild Corp.1979-11-05
TEW BYPASS INSTRUMENTS & DISSECTING KIT (K791703)Edward Weck, Inc.1979-10-04

Recalls involving this device

No recalls on record reference this clearance.