FDA 510(k)

EYE CARE TRAY

K-Number: K811117 · 1981-07-16

Decision Date1981-07-16

Product Code

DecisionSubstantially Equivalent

Device Summary

EYE CARE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1981-07-16 under 510(k) number K811117. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EYE CARE TRAY?

EYE CARE TRAY is a medical device that received FDA 510(k) clearance on 1981-07-16. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K811117.

When did EYE CARE TRAY receive FDA 510(k) clearance?

EYE CARE TRAY received FDA 510(k) clearance on 1981-07-16, under 510(k) number K811117.

Who is the listed applicant for EYE CARE TRAY?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

Other records listing American Pharmaseal Div. Ahsc 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.

K874022PHARMASEAL WOUND IRRIGATION DEVICE K874517PHARMASEAL RUBBER URETHRAL CATHETER K874045PHARMASEAL ENDOSCOPY PREP KIT UPPER AND LOWER K873359AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE K872228PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM K872917JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER

View all 64 devices →

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.