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FDA 510(k)

CROWNTEX EXAM. CAPE & GOWN

K-Number: K760954 · 1976-12-30

ApplicantGraham Manufacturing Co.
Decision Date1976-12-30
Product CodeFME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CROWNTEX EXAM. CAPE & GOWN is the device name listed in this FDA 510(k) record. The listed applicant is Graham Manufacturing Co.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K760954. The device is classified under product code FME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROWNTEX EXAM. CAPE & GOWN?

CROWNTEX EXAM. CAPE & GOWN is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Graham Manufacturing Co.. The 510(k) number is K760954.

When did CROWNTEX EXAM. CAPE & GOWN receive FDA 510(k) clearance?

CROWNTEX EXAM. CAPE & GOWN received FDA 510(k) clearance on 1976-12-30, under 510(k) number K760954.

Who is the listed applicant for CROWNTEX EXAM. CAPE & GOWN?

The FDA 510(k) record lists Graham Manufacturing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CROWNTEX EXAM. CAPE & GOWN?

The FDA product code for CROWNTEX EXAM. CAPE & GOWN is FME.

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Related Devices (Code: FME)

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.

K880385KIMBERLY-CLARK PROFESSIONAL JACKETKimberly-Clark Corp.K811915MONITOR/VITAL SIGNS TRAYAmerican Hospital Supply Corp.K770476EXAM GOWNGeneral Medical Co.K760360SHIRT, MITTEN CUFF INFANTPrecept, Inc.

Official Source

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

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