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FDA 510(k)

TAPE, LIGHTCAST II WB

K-Number: K760413 · 1976-08-23

ApplicantSolar Laboratories, Inc.
Decision Date1976-08-23
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TAPE, LIGHTCAST II WB 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 1976-08-23 under 510(k) number K760413. 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 TAPE, LIGHTCAST II WB?

TAPE, LIGHTCAST II WB is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Solar Laboratories, Inc.. The 510(k) number is K760413.

When did TAPE, LIGHTCAST II WB receive FDA 510(k) clearance?

TAPE, LIGHTCAST II WB received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760413.

Who is the listed applicant for TAPE, LIGHTCAST II WB?

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 TAPE, LIGHTCAST II WB?

The FDA product code for TAPE, LIGHTCAST II WB 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.

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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-PHENYLACETOPHENONEK770134LIGHTCAST II STOCKINETTEK770133LIGHTCAST II CASTING SYSTEM (MODIFIED)K761222BENZOIN ISOBUTYL ETHER

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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