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510(k) K771239

GOAT LAMBDA-LIGHT CHAIN ANTIHUMAN SERUM by G.D. Searle And Co.

K771239 is an FDA 510(k) premarket notification submitted by G.D. Searle And Co. for the device "GOAT LAMBDA-LIGHT CHAIN ANTIHUMAN SERUM". The FDA issued a decision of Substantially Equivalent on Aug 2, 1977. G.D. Searle And Co. has 55 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Aug 2, 1977
Date Received
Jul 11, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by G.D. Searle And Co.

  • K821159 — IN-LINE OXYGEN MONITORING SYSTEM (May 25, 1982)
  • K811068 — BYPASS COIL (May 27, 1981)
  • K811071 — VENOUS OXYGEN PROBE (May 5, 1981)
  • K803238 — INTRAVASCULAR CATHETER (Apr 23, 1981)
  • K810630 — SILICONE ELASTOMER COATED LATEX FOLEY (Mar 31, 1981)
  • K810131 — ADMINISTRATION SET (Feb 26, 1981)
  • K802485 — SEARLE VASCULAR LOOPS (Feb 12, 1981)
  • K801805 — METRONIDAZOLE DISCS (Feb 10, 1981)
  • K810112 — SWR DISPOSABLE PREP RAZOR (Feb 4, 1981)
  • K802280 — WHITE KNIGHT DRAPE SEAL (Oct 10, 1980)

FDA data resources

Source: FDA 510(k) database entry for K771239. Report a data issue: hello@regdatalab.com.