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FDA 510(k)

CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL

K-Number: K021676 · 2002-07-12

ApplicantCypress Medical Products, Ltd.
Decision Date2002-07-12
Product CodeHIB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL is the device name listed in this FDA 510(k) record. The listed applicant is Cypress Medical Products, Ltd.. It received FDA 510(k) clearance on 2002-07-12 under 510(k) number K021676. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL?

CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL is a medical device that received FDA 510(k) clearance on 2002-07-12. The listed applicant is Cypress Medical Products, Ltd.. The 510(k) number is K021676.

When did CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL receive FDA 510(k) clearance?

CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL received FDA 510(k) clearance on 2002-07-12, under 510(k) number K021676.

Who is the listed applicant for CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL?

The FDA 510(k) record lists Cypress Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL?

The FDA product code for CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL is HIB.

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Other records listing Cypress Medical Products, Ltd. as applicant

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Related Devices (Code: HIB)

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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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