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FDA 510(k)

PRECISION CAP STRAPS

K-Number: K830602 · 1983-03-24

ApplicantPrecision Cap Systems
Decision Date1983-03-24
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PRECISION CAP STRAPS is the device name listed in this FDA 510(k) record. The listed applicant is Precision Cap Systems. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830602. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION CAP STRAPS?

PRECISION CAP STRAPS is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Precision Cap Systems. The 510(k) number is K830602.

When did PRECISION CAP STRAPS receive FDA 510(k) clearance?

PRECISION CAP STRAPS received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830602.

Who is the listed applicant for PRECISION CAP STRAPS?

The FDA 510(k) record lists Precision Cap Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRECISION CAP STRAPS?

The FDA product code for PRECISION CAP STRAPS is GXY.

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Other records listing Precision Cap Systems 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.

K830598EVOKED POTENTIAL CAP W/EVOKED POTENTIALK830597BABY CAP, ELECTRODE SET & BOARD ADAPTORK830599LOCALIZING ELECTRODEK830601FOAMIES DIAPOS. FOAM RUBBER PADSK830521PRECISION EEG CAP W/ELECTRODE SET ANDK830600REFERENCE & MONITORING ELECTRODE

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Related Devices (Code: GXY)

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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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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