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FDA 510(k)

LIDSPLINT

K-Number: K864810 · 1987-01-20

ApplicantPrecision Therapeutics, Inc.
Decision Date1987-01-20
Product CodeHMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIDSPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Precision Therapeutics, Inc.. It received FDA 510(k) clearance on 1987-01-20 under 510(k) number K864810. The device is classified under product code HMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIDSPLINT?

LIDSPLINT is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is Precision Therapeutics, Inc.. The 510(k) number is K864810.

When did LIDSPLINT receive FDA 510(k) clearance?

LIDSPLINT received FDA 510(k) clearance on 1987-01-20, under 510(k) number K864810.

Who is the listed applicant for LIDSPLINT?

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

What is the FDA product code for LIDSPLINT?

The FDA product code for LIDSPLINT is HMP.

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 Precision Therapeutics, 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.

K872659TAPELESS EYE SHIELD

Related Devices (Code: HMP)

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.

K940333EYE PADCertified Safety Mfg., Inc.K921349STERILE,DISPOSABLE EYE DRESSINGDeroyal Industries, Inc.K904896EYE PADUlti-Med Intl., Inc.K883822FIRST AID KIT, EYE DRESSING NSN6545-00-853-6309Consolidated Industries of Greater Syracuse, Inc.K874411DONALDSON NATURAL EYEPATCH 'PATIENT PAK'Keeler Instruments, Inc.K861456SHEETS LYOPHILIZED COLLAGEN HEYEDRATORPantheon Products, 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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