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FDA 510(k)

FIBER OPTIC ADJUSTABLE HEADLIGHT

K-Number: K780433 · 1978-06-13

ApplicantCameron-Miller, Inc.
Decision Date1978-06-13
Product CodeFCT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC ADJUSTABLE HEADLIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Cameron-Miller, Inc.. It received FDA 510(k) clearance on 1978-06-13 under 510(k) number K780433. The device is classified under product code FCT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC ADJUSTABLE HEADLIGHT?

FIBER OPTIC ADJUSTABLE HEADLIGHT is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K780433.

When did FIBER OPTIC ADJUSTABLE HEADLIGHT receive FDA 510(k) clearance?

FIBER OPTIC ADJUSTABLE HEADLIGHT received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780433.

Who is the listed applicant for FIBER OPTIC ADJUSTABLE HEADLIGHT?

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

What is the FDA product code for FIBER OPTIC ADJUSTABLE HEADLIGHT?

The FDA product code for FIBER OPTIC ADJUSTABLE HEADLIGHT is FCT.

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Other records listing Cameron-Miller, 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.

K944775ELECTROSURGICAL UNIT MODEL 26-0335K931541MODEL 26-0375, ELECTROSURGICAL GENERATORK931437MODEL 80-1983, ELECTROSURGICAL GENERATORK935490ELECTROSURGICAL DEVICE, MODEL 26-2500K854109ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345K853972CAMERON-MILLER MODEL 80-2701, BIPOLAR COAGULATOR

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Related Devices (Code: FCT)

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.

K960767LIGHT COMMANDERScieran Technologies, Inc.K924198MODIFIED SITE FIBER OPTIC MODULEChiron Vision Corp.K883480MODIFIED SITE FIBER OPTIC MODULE FOR OPHTHAL. USESite Microsurgical Systems, Inc.K802769FIBER OPTIC HEADLIGHT #60-0765Aspen Laboratories, Inc.K802770FIBER OPTIC HEADLIGHT #60-0766766Aspen Laboratories, 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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