Atlas FDA

V LANCE

FDA 510(k) clearance K821440 · decided 1982-06-14

Clearance details

K-number
K821440
Device name
V LANCE
Applicant
Sharpoint, Inc.
Decision
Substantially Equivalent
Date received
1982-05-13
Decision date
1982-06-14
Days to decision
32 days
Clearance type
Traditional
Product code
HNN
Device class
1
Regulation number
886.4350
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Walker, MI, 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
CLEARCUT S SAFETY KNIFE (K110166)Alcon Research, Ltd.2011-05-20
OPHTHALMIC KNIFE (K922378)Microptics Development Laboratory1992-12-10
RETRACTIVE INCISION MICROMETER (RIM) GUAGE (K882402)Optical Center1988-08-22
MVR/STILETTO BLADE 20GA. - P/N 1900 (K881669)Advanced Surgical Products, Inc.1988-05-13
PRISMA DISPOSABLE MVR/STILETTO BLADE (K874979)Advanced Surgical Products, Inc.1988-04-13
OPHTHALMIC TIP & BLADE SCALPELS (K874057)Myocure, Inc.1987-12-23
OPHTHALMIC DISPOSABLE BLADES (K874056)Myocure, Inc.1987-12-22
OPHTHALMIC PHACO-BLADE (K873385)Myocure, Inc.1987-09-21
KNIFE, OPHTHALMIC (K871285)Trueline Instruments, Inc.1987-04-27
RK-M & RK-DK DIAMOND KNIVES WITH MEASURING GAUGE (K864290)Keeler Instruments, Inc.1986-12-15
CATARACT DIAMOND KNIFE (K863725)Medical Technology Development Corp.1986-10-31
THE ULTIMATE (K863665)Myocure, Inc.1986-09-25

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
SILK SURGICAL SUTURES (N85143/S004)Sharpoint, Inc.1988-08-31
SILK SURGICAL SUTURES (N85143/S007)Sharpoint, Inc.1988-07-19
SILK SURGICAL SUTURES (N85143/S006)Sharpoint, Inc.1988-03-22
SILK SURGICAL SUTURES (N85143/S005)Sharpoint, Inc.1987-10-13
SUTURES (N85143/S003)Sharpoint, Inc.1987-08-27
SUTURES (N85143/S002)Sharpoint, Inc.1987-04-03
SUTURES (N85143/S001)Sharpoint, Inc.1986-10-27