Atlas FDA

CONPHAR O.R. HEAD COVER-STERILE

FDA 510(k) clearance K792106 · decided 1979-11-05

Clearance details

K-number
K792106
Device name
CONPHAR O.R. HEAD COVER-STERILE
Applicant
Conphar, Inc.
Decision
Substantially Equivalent
Date received
1979-10-25
Decision date
1979-11-05
Days to decision
11 days
Clearance type
Traditional
Product code
FYI
Device class
1
Regulation number
878.3250
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
OMEGA BIVALVE NASAL SPLINTS (K871073)Omega Silicone, Inc.1987-05-11
ETHICON EXTERNAL FIXATION WIRE (K821178)ETHICON, Inc.1983-06-11
STRAITH NASAL SPLINT (K801072)Surgical Technology Laboratories, Inc.1980-06-17

Recalls involving this device

No recalls on record reference this clearance.