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FDA 510(k)

CUTTER CAST 7

K-Number: K770742 · 1977-04-28

ApplicantCutter Laboratories, Inc.
Decision Date1977-04-28
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CUTTER CAST 7 is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1977-04-28 under 510(k) number K770742. The device is classified under product code ITG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTTER CAST 7?

CUTTER CAST 7 is a medical device that received FDA 510(k) clearance on 1977-04-28. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K770742.

When did CUTTER CAST 7 receive FDA 510(k) clearance?

CUTTER CAST 7 received FDA 510(k) clearance on 1977-04-28, under 510(k) number K770742.

Who is the listed applicant for CUTTER CAST 7?

The FDA 510(k) record lists Cutter Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUTTER CAST 7?

The FDA product code for CUTTER CAST 7 is ITG.

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Other records listing Cutter Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K861315HYPERBARIC PENETRATION EXTENSION SETK854106BAYSILEXK842324PERFOURMK834106INTRAVENOUS INFUSION CONTROLLERK832237ORTHOPEDIC CASTING TAPE MAXCASTK823214DOSIMETRIC RELEASE PROGRAM - ADMIN. SET

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Related Devices (Code: ITG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K873111CONFORMA(TM) PLASTER BANDAGESThe Kendal Co.K862115DEKNA BAND KITDeknatel, Inc.K842573T.P.G. CAST TAPEThe Poly Group, Inc.K840416HEXCELITEHexcel MedicalK833732NON WETTING UNDERCAST PADDINGAmerican Medical Disposable, Inc.K832992SOFFBAN ORTHOPEDIC PADDINGSmith & Nephew, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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