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FDA 510(k)

LIGHTCAST II STOCKINETTE

K-Number: K770134 · 1977-01-26

ApplicantSolar Laboratories, Inc.
Decision Date1977-01-26
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIGHTCAST II STOCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Solar Laboratories, Inc.. It received FDA 510(k) clearance on 1977-01-26 under 510(k) number K770134. 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 LIGHTCAST II STOCKINETTE?

LIGHTCAST II STOCKINETTE is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Solar Laboratories, Inc.. The 510(k) number is K770134.

When did LIGHTCAST II STOCKINETTE receive FDA 510(k) clearance?

LIGHTCAST II STOCKINETTE received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770134.

Who is the listed applicant for LIGHTCAST II STOCKINETTE?

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

What is the FDA product code for LIGHTCAST II STOCKINETTE?

The FDA product code for LIGHTCAST II STOCKINETTE is ITG.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Solar 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.

K7712442,2DIMETHOXY-2-PHENYLACETOPHENONEK770133LIGHTCAST II CASTING SYSTEM (MODIFIED)K761222BENZOIN ISOBUTYL ETHERK760413TAPE, LIGHTCAST II WB

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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